CN102036650A - Surface-treated powder and cosmetic comprising the same - Google Patents
Surface-treated powder and cosmetic comprising the same Download PDFInfo
- Publication number
- CN102036650A CN102036650A CN2009801184599A CN200980118459A CN102036650A CN 102036650 A CN102036650 A CN 102036650A CN 2009801184599 A CN2009801184599 A CN 2009801184599A CN 200980118459 A CN200980118459 A CN 200980118459A CN 102036650 A CN102036650 A CN 102036650A
- Authority
- CN
- China
- Prior art keywords
- chemical compound
- comparative example
- treated powder
- powder
- fluorinated copolymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/11—Encapsulated compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8123—Compositions of homopolymers or copolymers of compounds having one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers, e.g. PVC, PTFE
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
- A61Q1/06—Lipsticks
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/12—Face or body powders for grooming, adorning or absorbing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/008—Preparations for oily skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q3/00—Manicure or pedicure preparations
- A61Q3/02—Nail coatings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/0015—Pigments exhibiting interference colours, e.g. transparent platelets of appropriate thinness or flaky substrates, e.g. mica, bearing appropriate thin transparent coatings
- C09C1/0021—Pigments exhibiting interference colours, e.g. transparent platelets of appropriate thinness or flaky substrates, e.g. mica, bearing appropriate thin transparent coatings comprising a core coated with only one layer having a high or low refractive index
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/04—Compounds of zinc
- C09C1/043—Zinc oxide
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/22—Compounds of iron
- C09C1/24—Oxides of iron
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/36—Compounds of titanium
- C09C1/3607—Titanium dioxide
- C09C1/3676—Treatment with macro-molecular organic compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/40—Compounds of aluminium
- C09C1/42—Clays
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/10—Treatment with macromolecular organic compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C2200/00—Compositional and structural details of pigments exhibiting interference colours
- C09C2200/10—Interference pigments characterized by the core material
- C09C2200/102—Interference pigments characterized by the core material the core consisting of glass or silicate material like mica or clays, e.g. kaolin
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C2200/00—Compositional and structural details of pigments exhibiting interference colours
- C09C2200/40—Interference pigments comprising an outermost surface coating
- C09C2200/402—Organic protective coating
- C09C2200/405—High molecular weight materials, e.g. polymers
- C09C2200/406—High molecular weight materials, e.g. polymers comprising additional functional groups, e.g. -NH2, -C=C- or -SO3
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dispersion Chemistry (AREA)
- Cosmetics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Provided is a surface-treated powder which is excellent in terms of usability and is highly adhesive to skin. This powder is coated with a surface-treating agent which comprises a fluorine-containing copolymer consisting of (a) a fluorine-containing monomer represented by general formula (I) and (b) an alkoxy-containing monomer represented by general formula (II). This powder is usable in various cosmetics. CH2=C(-X)-C(=O)-Y-[-(CH2)m-Z-]p-(CH2)n-Rf (I) CH2=C(X1)-C(=O)-O-(RO)q-X2 (II).
Description
Technical field
The present invention relates to a kind of surface-treated powder, at least a portion surface that specifically relates to powder particle is comprised the surface-treated powder that chemical compound was covered of specific fluorinated copolymer at least and is contained cosmetics of this surface-treated powder etc.
The usability of surface-treated powder of the present invention, with the adaptation excellence of skin, and with cosmetic formulations in the affinity excellence of other composition of being mixed.Be mixed with the cosmetics of this surface-treated powder usability, make up finish effect, cosmetic persistence and quality stability, to organism and environmentAL safety excellence.
In addition, surface-treated powder of the present invention is preferably and can be used as the used for cosmetic surface-treated powder, but it not only can be applicable to cosmetics, various fields such as the powder body filler that also can be applicable in ink, coating, resin concentrates, the paper etc. to be mixed, ceramic material, magnetic material, rare earth, optical material, conductive material, voltage material.
Background technology
In the past, handled powder body, and disclosed and utilize perfluoralkyl phosphate, perfluoroalkyl silane to carry out surface-treated powder body (patent documentation 1 and patent documentation 2) as employed fluorochemical in the cosmetics.Though handling powder body, these have water and oil repellant, and have patience from oozy antiperspirant of skin and sebum, but poor with the affinity of other used for cosmetic raw material, aspect preparationization, there is sizable restriction, still have some deficits at usability with aspect the adaptation of skin.In addition, can repel in air as oily sebum though these handle powder body, in the system (under the environment that easily perspire summer) of antiperspirant and sebum coexistence, these oil repellents (anti-sebum) of handling powder body can weaken, and have problems aspect the cosmetic persistence.As the surface-treated powder that has solved this problem, disclose perfluoroalkyl acrylate and silicone macromolecule monomer (silicone macromer) are arranged, the surface-treated powder (patent documentation 3) of the fluorinated copolymer of polyalkene glycol acrylates.Yet, if in molecule, introduce siloxane chain (silicone chain), the shortcoming that has oil repellent to reduce.In addition, disclose the surface-treated powder of the copolymer that perfluoroalkyl acrylate and polyalkene glycol acrylates are arranged in the patent documentation 4, the embodiment of its description discloses: carbon number is in the water of combination of fluoro-alkyl below 6 and methacrylic acid hydroxyl ethyl ester (HEMA) a little less than the oil repellent (patent documentation 4).
In recent years, think contain carbon number be the chemical compound of the fluoro-alkyl more than 8 by decomposing or metabolism may generate as the perfluoro caprylic acid (PFOA) that contains carboxylic acid fluoride, therefore more and more worry and can produce burden environment.In view of this situation, as the fluorinated alkyl compound that is used for powder handling, bringing into use carbon number is that short chain compound below 6 replaces the above-mentioned chemical compound that carbon number is the fluoro-alkyl more than 8 that contains.For example, disclose and to have that to have carbon number be the fluoro-alkyl below 6 and the fluorinated copolymer or the fluoroalkyl silanes (patent documentation 5 and patent documentation 6) of water and oil repellant excellence.
In order to realize water and oil repellant, disclosing has the graft copolymer that has fluorine segment and hydrophilic segment in the molecule.In addition, announcement has the polymer (patent documentation 7 and patent documentation 8) that has enough dissolubilities and resistance to water, flexibility and epithelium excellent strength in water.
Patent documentation 1: the Japan Patent spy opens clear 62-250074 communique
Patent documentation 2: Japanese patent laid-open 2-218603 communique
Patent documentation 3: the Japan Patent spy opens the 2008-50620 communique
Patent documentation 4: the Japan Patent spy opens the 2000-290640 communique
Patent documentation 5: the Japan Patent spy opens the 2007-210939 communique
Patent documentation 6: the Japan Patent spy opens the 2007-238690 communique
No. 95/18194 communique of patent documentation 7:WO
Patent documentation 8: the Japan Patent spy opens the 2005-213485 communique
The announcement of invention
Yet the existing fluorine that demonstrates water and oil repellant is handled dissolubility, emulsibility, the bad dispersibility of powder body and other used for cosmetic raw material, has the little problem of accommodation of preparationization.In addition, existing fluorochemical handle powder body have water and oil repellant and usability good, have with the adaptation of the excellence of skin, usability is excellent and have concurrently to make up to finish and still have some deficits aspect effect and the cosmetic persistence when being used for cosmetics, and then does not still have the fluorochemical processing powder body of considering organism and environmentAL safety that carbon number is the fluoro-alkyl below 6 that has.In addition, still do not have with cosmetic formulations in other composition of being mixed the affinity excellence have a fluorochemical processing powder body that carbon number is the fluoro-alkyl 6 below.Therefore, require to develop the affinity excellence of other composition that is mixed in a kind of and the cosmetic formulations and oil repellent and the usability excellence in cosmetics, have concurrently to make up and finish effect and cosmetic persistence and consider surface-treated powder organism and environmentAL safety.
The object of the present invention is to provide a kind of usability, handle powder body with the fluorochemical of the adaptation excellence of skin, and a kind of cosmetics that are mixed with surface-treated powder of the present invention are provided, the usability of these cosmetics, make up finish effect, cosmetic persistence, quality stability, to organism and environmentAL safety excellence.
The inventor concentrates on studies in order to solve above-mentioned problem, and found that: the surface-treated powder that chemical compound was covered that is comprised specific fluorinated copolymer at least can be realized this purpose.Above-mentioned specific fluorinated copolymer be must comprise the fluorochemical monomer shown in (a) following general formula (I) and (b) the monomeric monomer copolymerization that contains alkoxyl shown in the following general formula (II) and fluorinated copolymer.
(1) promptly, the present invention can provide a kind of surface-treated powder, it is to desire to carry out the surface-treated powder that the surface of surface-treated powder particle forms with surface conditioning agent lining, it is characterized in that, above-mentioned surface conditioning agent be must comprise the fluorochemical monomer shown in (a) following general formula (I) and (b) the monomeric monomer copolymerization that contains alkoxyl shown in the following general formula (II) and fluorinated copolymer;
CH
2＝C(-X)-C(＝O)-Y-[-(CH
2)
m-Z-]
p-(CH
2)
n-Rf (I)
In the formula, X is hydrogen atom, methyl, fluorine atom, chlorine atom, bromine atoms, iodine atom, CFX
1X
2Base (wherein, X
1And X
2Be hydrogen atom, fluorine atom or chlorine atom), cyano group, carbon number be 1～20 straight chain shape or branch-like fluoro-alkyl, be substituted or the benzyl of non-replacement, be substituted or the phenyl of non-replacement;
Y is-O-or-NH-;
Z be Direct Bonding ,-S-or-SO
2-;
Rf is that carbon number is 1～6 fluoro-alkyl;
M is 1～10, and n is 0～10, and p is 0 or 1;
CH
2＝C(X
1)-C(＝O)-O-(RO)
q-X
2 (II)
In the formula, X
1Be hydrogen atom or methyl;
X
2It for hydrogen atom or carbon number 1～22 unsaturated or saturated hydrocarbyl;
R is that carbon number that part or all of hydrogen atom can be replaced by hydroxyl is 2～4 alkylidene;
Q is 1～50 integer.
The preferred configuration of surface-treated powder of the present invention can be enumerated following form.
(2) as (1) described surface-treated powder, wherein, in the above-mentioned general formula (II), X
2Be hydrogen atom.
(3) as (1) or (2) described surface-treated powder, wherein, above-mentioned surface-treated powder has water and oil repellant.
(4) as (1) or (2) described surface-treated powder, wherein, above-mentioned surface-treated powder has hydrophilic water repellency.
(5) as each described surface-treated powder in (1) to (4), the fluorinated copolymer that comprises the cross-linkable monomer shown in the following logical formula III in its constituent by above-mentioned fluorinated copolymer is covered;
CH
2＝C(X
3)-C(＝O)-O-(R
1O)
q-C(＝O)-C(X
3)＝CH
2 (III)
In the formula, each X
3Be hydrogen atom or methyl; R
1The carbon number that can be replaced by hydroxyl for part or all of hydrogen atom is 2～10 alkylidene; Q is 1～50 integer.
(6) as each described surface-treated powder in (1) to (5), wherein, the weight average molecular weight of above-mentioned fluorinated copolymer is about 1000～about 1000000.
(7) as each described surface-treated powder in (1) to (6), wherein, in the above-mentioned fluorinated copolymer, fluorochemical monomer (a) is 100 weight portions, and the monomer (b) that contains alkoxyl is 10～400 weight portions.
(8) as each described surface-treated powder in (1) to (7), wherein, desire to carry out surface-treated powder body 100 weight portions with respect to above-mentioned, the amount of coating of above-mentioned fluorinated copolymer is 0.01～40 weight portion.
(9) as each described surface-treated powder in (1) to (8), wherein, above-mentioned surface conditioning agent also comprises more than one the chemical compound that is selected from the following chemical compound group;
Above-claimed cpd group: other fluorochemical, organopolysiloxane, alkyl silane, polyether modified silicane, organic titanate, polyolefin, hydrolecithin (hydrolecithin that comprises the salt form), acylated amino acid (acylated amino acid that comprises salt form or compositions form), acid ester oil, fatty acid (fatty acid that comprises the salt form) and dextrin fatty acid ester beyond the above-mentioned fluorinated copolymer.
(10) as (9) described surface-treated powder, wherein, above-mentioned fluorochemical is that carbon number is at least a in perfluoralkyl phosphate below 6 and perfluoroalkyl silane, perfluoro polyether phosphate, the Perfluoropolyether silanes.
(11) as each described surface-treated powder in (1) to (10), it is by desiring to carry out surface-treated powder body 100 weight portions and be covered by more than one the chemical compound that is selected from the above-claimed cpd group of the above-mentioned fluorinated copolymer of 0.01 weight portion～39.99 weight portions and 39.99 weight portions～0.01 weight portion with respect to above-mentioned.
(12) as each described surface-treated powder in (1) to (11), wherein, above-mentioned to desire to carry out the surface-treated powder body be the powder body that can be used for cosmetics.
(13) as (12) described surface-treated powder, wherein, the powder body that can be used for above-mentioned cosmetics is the inorganic particle that can be used for cosmetics.
(14) as (13) described surface-treated powder, wherein, above-mentioned inorganic particle be in sericite (sericite), Muscovitum (mica), Kaolin (kaolin), Talcum (talc), silicon dioxide (silica), barium sulfate, boron nitride, titanium oxide, zinc oxide, ferrum oxide and the pearlescent pigment any or two or more.
(15) as (12) described surface-treated powder, wherein, the powder body that can be used for above-mentioned cosmetics is the organic powder that can be used for cosmetics.
With regard to another viewpoint of the present invention, a kind of cosmetics can be provided, it is characterized in that containing above-mentioned surface-treated powder, be surface-treated powder of the present invention.Cosmetics of the present invention are preferably except that this surface-treated powder, also comprise at least a as constituent in oiliness composition, water composition and the surfactant.
In addition, cosmetics of the present invention are preferably any cosmetic in skin care (skin care) cosmetics, cosmetic hair, cosmetic (make-up) cosmetics and the uvioresistant cosmetics.That the goods form is preferably is aqueous, any form in emulsion form, white shape, solid shape, pasty state, gel, Powdered, multilamellar shape, Mu Si (mousse) shape and the spray form.
The invention provides a kind of usability, with the adaptation excellence of skin, and with cosmetic formulations in the surface-treated powder of affinity excellence of other composition of being mixed, a kind of used for cosmetic surface-treated powder especially is provided.Surface-treated powder of the present invention can be water and oil repellant or hydrophilic oil repellent.Here, above-mentioned water and oil repellant is meant the conformation (conformation) that changes polymer molecule by the lining method of above-mentioned specific fluorinated copolymer and amount of coating, makes surface-treated powder show water repellency and oil repellent by this.Can make the surface conditioning agent of water and oil repellant or hydrophilic oil repellent according to purpose and purposes etc.Above-mentioned hydrophilic oil repellent is meant the conformation that changes polymer molecule by the lining method of above-mentioned specific fluorinated copolymer and amount of coating, makes surface-treated powder show hydrophilic and oil repellent by this.According to the kind of the powder body that is covered and the condition of processing, show water repellency or hydrophilic amount of coating difference.Hydrophilic oil repellent powder body of the present invention not only can mix in the water composition of cosmetics, also can be used as emulsion adjuvant, and the accommodation of preparationization greatly enlarges.
In addition, by mixing surface-treated powder of the present invention, can be easily and make usability easily, make up and to finish effect and the good cosmetics of cosmetic persistence.In addition, about being mixed with the cosmetics of above-mentioned surface-treated powder, its anti-sebum and anti-transfer printing excellence, and given play to the effect that prevents the agglutinative effect of powder body, suppress catalyst activity, prevent by with the caused fouling of interaction of organic uv absorbers etc. or painted effect, prevent effect that crystallization separates out, prevent and reactive effect of water-soluble thickener, suppress the effect of moisture loss etc.In addition, the quality stability of cosmetics and safety greatly promote because of these effects.Therefore, the present invention is especially at cosmetic field, industrial extremely useful.
The best mode that carries out an invention
Below, be the center with the situation that surface-treated powder of the present invention is particularly useful for cosmetic use, be elaborated to implementing best mode of the present invention, but be not limited to these modes.In addition, among the present invention, desire to carry out any form that the surface-treated powder body comprises powder body and particle.
(surface-treated powder of the present invention)
Surface-treated powder of the present invention is a surface-treated powder, is preferably the used for cosmetic surface-treated powder, and at least a portion of desiring to carry out the surface of surface-treated powder particle is covered by the surface conditioning agent of the chemical compound that comprises specific fluorinated copolymer at least.
Employed surface conditioning agent is specific fluorinated copolymer among the present invention.This fluorinated copolymer be must comprise the fluorochemical monomer shown in (a) following general formula (I) and (b) the monomeric monomer copolymerization that contains alkoxyl shown in the following general formula (II) and.
Fluorochemical monomer (a):
CH
2＝C(-X)-C(＝O)-Y-[-(CH
2)
m-Z-]
p-(CH
2)
n-Rf (I)
In the formula, X is that hydrogen atom, methyl, carbon number are 1～21 the straight chain shape or alkyl, fluorine atom, chlorine atom, bromine atoms, iodine atom, the CFX of branch-like
1X
2Base (wherein, X
1And X
2Be hydrogen atom, fluorine atom, chlorine atom, bromine atoms or iodine atom), cyano group, carbon number be 1～20 straight chain shape or branch-like fluoro-alkyl, be substituted or the benzyl of non-replacement, be substituted or the phenyl of non-replacement;
Y is-O-or-NH-;
Z be Direct Bonding ,-S-or-SO
2-;
Rf is that carbon number is 1～6 fluoro-alkyl;
M is 1～10, and n is 0～10, and p is 0 or 1.The monomer (b) that contains alkoxyl is represented with general formula (II):
CH
2＝C(X
1)-C(＝O)-O-(R
1O)
q-X
2 (II)
In the formula, X
1Be hydrogen atom or methyl;
X
2It for hydrogen atom or carbon number 1～22 unsaturated or saturated hydrocarbyl;
R
1The carbon number that can be replaced by hydroxyl for part or all of hydrogen atom is 2～4 alkylidene;
Q is 1～50 integer.
In the above-mentioned general formula (I), being preferably p is 0.The preference of X is a hydrogen atom.
Fluorochemical monomer (a) generally has perfluoroalkyl and/or partially fluorinated fluoro-alkyl.Be preferably perfluoroalkyl.The carbon number of Rf base is 1～6.The carbon number of Rf base is preferably 4,5 or 6, and especially good is 6.The example of Rf base has :-CF
3,-CF
2CF
3,-CF
2CF
2CF
3,-CF (CF
3)
2,-CF
2CF
2CF
2CF
3,-CF
2CF (CF
3)
2,-C (CF
3)
3,-(CF
2)
4CF
3,-(CF
2)
2CF (CF
3)
2,-CF
2C (CF
3)
3,-CF (CF
3) CF
2CF
2CF
3,-(CF
2)
5CF
3Deng.
Fluorochemical monomer (a) can use separately certainly, also can be use mixing two or more.
Fluorochemical monomer (a) for example can be listed below.
CH2＝C(-X)-C(＝O)-O-(CH2)m-S-(CH2)n-Rf
CH2＝C(-X)-C(＝O)-O-(CH2)m-SO2-(CH2)n-Rf
CH2＝C(-X)-C(＝O)-O-(CH2)n-Rf
CH2＝C(-X)-C(＝O)-NH-(CH2)n-Rf
In the above-mentioned formula, X is hydrogen atom, methyl, fluorine atom, chlorine atom, bromine atoms, iodine atom, CFX
1X
2Base (wherein, X
1And X
2Be hydrogen atom, fluorine atom or chlorine atom), cyano group, carbon number be 1～20 straight chain shape or branch-like fluoro-alkyl, be substituted or the benzyl of non-replacement, be substituted or the phenyl of non-replacement;
Rf is 1～6 fluoro-alkyl;
M is 1～10, and n is 0～10.
The concrete example of fluorochemical monomer (a) for example can be listed below, but is not limited to these examples.
CH2＝C(-H)-C(＝O)-O-(CH2)2-S-Rf
CH2＝C(-H)-C(＝O)-O-(CH2)2-S-(CH2)2-Rf
CH2＝C(-H)-C(＝O)-O-(CH2)3-SO2-Rf
CH2＝C(-H)-C(＝O)-O-(CH2)2-SO2-(CH2)2-Rf
CH2＝C(-H)-C(＝O)-O-(CH2)2-Rf
CH2＝C(-H)-C(＝O)-NH-(CH2)2-Rf
CH2＝C(-H)-C(＝O)-OCH2CH2N(C2H5)SO2-Rf
CH2＝C(-H)-C(＝O)-OCH2CH2N(CH3)SO2-Rf
CH2＝C(-H)-C(＝O)-OCH2CH(OCOCH3)CH2-Rf
CH2＝C(-CH3)-C(＝O)-O-(CH2)2-S-Rf
CH2＝C(-CH3)-C(＝O)-O-(CH2)2-S-(CH2)2-Rf
CH2＝C(-CH3)-C(＝O)-O-(CH2)3-SO2-Rf
CH2＝C(-CH3)-C(＝O)-O-(CH2)2-SO2-(CH2)2-Rf
CH2＝C(-CH3)-C(＝O)-O-(CH2)2-Rf
CH2＝C(-CH3)-C(＝O)-NH-(CH2)2-Rf
CH2＝C(-CH3)-C(＝O)-OCH2CH2N(C2H5)SO2-Rf
CH2＝C(-CH3)-C(＝O)-OCH2CH2N(CH3)SO2-Rf
CH2＝C(-CH3)-C(＝O)-OCH2CH(OCOCH3)CH2-Rf
CH2＝C(-F)-C(＝O)-O-(CH2)2-S-Rf
CH2＝C(-F)-C(＝O)-O-(CH2)2-S-(CH2)2-Rf
CH2＝C(-F)-C(＝O)-O-(CH2)2-SO2-Rf
CH2＝C(-F)-C(＝O)-O-(CH2)2-SO2-(CH2)2-Rf
CH2＝C(-F)-C(＝O)-O-(CH2)2-Rf
CH2＝C(-F)-C(＝O)-NH-(CH2)2-Rf
CH2＝C(-Cl)-C(＝O)-O-(CH2)2-S-Rf
CH2＝C(-Cl)-C(＝O)-O-(CH2)2-S-(CH2)2-Rf
CH2＝C(-Cl)-C(＝O)-O-(CH2)2-SO2-Rf
CH2＝C(-Cl)-C(＝O)-O-(CH2)2-SO2-(CH2)2-Rf
CH2＝C(-Cl)-C(＝O)-O-(CH2)2-Rf
CH2＝C(-Cl)-C(＝O)-NH-(CH2)2-Rf
CH2＝C(-CF3)-C(＝O)-O-(CH2)2-S-Rf
CH2＝C(-CF3)-C(＝O)-O-(CH2)2-S-(CH2)2-Rf
CH2＝C(-CF3)-C(＝O)-O-(CH2)2-SO2-Rf
CH2＝C(-CF3)-C(＝O)-O-(CH2)2-SO2-(CH2)2-Rf
CH2＝C(-CF3)-C(＝O)-O-(CH2)2-Rf
CH2＝C(-CF3)-C(＝O)-NH-(CH2)2-Rf
CH2＝C(-CF2H)-C(＝O)-O-(CH2)2-S-Rf
CH2＝C(-CF2H)-C(＝O)-O-(CH2)2-S-(CH2)2-Rf
CH2＝C(-CF2H)-C(＝O)-O-(CH2)2-SO2-Rf
CH2＝C(-CF2H)-C(＝O)-O-(CH2)2-SO2-(CH2)2-Rf
CH2＝C(-CF2H)-C(＝O)-O-(CH2)2-Rf
CH2＝C(-CF2H)-C(＝O)-NH-(CH2)2-Rf
CH2＝C(-CN)-C(＝O)-O-(CH2)2-S-Rf
CH2＝C(-CN)-C(＝O)-O-(CH2)2-S-(CH2)2-Rf
CH2＝C(-CN)-C(＝O)-O-(CH2)2-SO2-Rf
CH2＝C(-CN)-C(＝O)-O-(CH2)2-SO2-(CH2)2-Rf
CH2＝C(-CN)-C(＝O)-O-(CH2)2-Rf
CH2＝C(-CN)-C(＝O)-NH-(CH2)2-Rf
CH2＝C(-CF2CF3)-C(＝O)-O-(CH2)2-S-Rf
CH2＝C(-CF2CF3)-C(＝O)-O-(CH2)2-S-(CH2)2-Rf
CH2＝C(-CF2CF3)-C(＝O)-O-(CH2)2-SO2-Rf
CH2＝C(-CF2CF3)-C(＝O)-O-(CH2)2-SO2-(CH2)2-Rf
CH2＝C(-CF2CF3)-C(＝O)-O-(CH2)2-Rf
CH2＝C(-CF2CF3)-C(＝O)-NH-(CH2)2-Rf
CH2＝C(-F)-C(＝O)-O-(CH2)3-S-Rf
CH2＝C(-F)-C(＝O)-O-(CH2)3-S-(CH2)2-Rf
CH2＝C(-F)-C(＝O)-O-(CH2)3-SO2-Rf
CH2＝C(-F)-C(＝O)-O-(CH2)3-SO2-(CH2)2-Rf
CH2＝C(-F)-C(＝O)-O-(CH2)3-Rf
CH2＝C(-F)-C(＝O)-NH-(CH2)3-Rf
CH2＝C(-Cl)-C(＝O)-O-(CH2)3-S-Rf
CH2＝C(-Cl)-C(＝O)-O-(CH2)3-S-(CH2)2-Rf
CH2＝C(-Cl)-C(＝O)-O-(CH2)3-SO2-Rf
CH2＝C(-Cl)-C(＝O)-O-(CH2)3-SO2-(CH2)2-Rf
CH2＝C(-CF3)-C(＝O)-O-(CH2)3-S-Rf
CH2＝C(-CF3)-C(＝O)-O-(CH2)3-S-(CH2)2-Rf
CH2＝C(-CF3)-C(＝O)-O-(CH2)3-SO2-Rf
CH2＝C(-CF3)-C(＝O)-O-(CH2)3-SO2-(CH2)2-Rf
CH2＝C(-CF2H)-C(＝O)-O-(CH2)3-S-Rf
CH2＝C(-CF2H)-C(＝O)-O-(CH2)3-S-(CH2)2-Rf
CH2＝C(-CF2H)-C(＝O)-O-(CH2)3-SO2-Rf
CH2＝C(-CF2H)-C(＝O)-O-(CH2)3-SO2-(CH2)2-Rf
CH2＝C(-CN)-C(＝O)-O-(CH2)3-S-Rf
CH2＝C(-CN)-C(＝O)-O-(CH2)3-S-(CH2)2-Rf
CH2＝C(-CN)-C(＝O)-O-(CH2)3-SO2-Rf
CH2＝C(-CN)-C(＝O)-O-(CH2)3-SO2-(CH2)2-Rf
CH2＝C(-CF2CF3)-C(＝O)-O-(CH2)3-S-Rf
CH2＝C(-CF2CF3)-C(＝O)-O-(CH2)3-S-(CH2)2-Rf
CH2＝C(-CF2CF3)-C(＝O)-O-(CH2)3-SO2-Rf
CH2＝C(-CF2CF3)-C(＝O)-O-(CH2)2-SO2-(CH2)2-Rf
In the above-mentioned formula, Rf is 1～6 fluoro-alkyl.
The monomer (b) that contains alkoxyl is non-fluorine monomer, is the chemical compound shown in the following general formula (II) (aklylene glycol (methyl) acrylate).
CH
2＝C(X
1)-C(＝O)-O-(RO)
q-X
2 (II)
In the formula, X
1Be hydrogen atom or methyl, X
2For hydrogen atom or carbon number are 1～22 unsaturated or saturated hydrocarbyl, R is that carbon number that part or all of hydrogen atom can be replaced by hydroxyl is 2～4 alkylidene; Q is 1～50 integer.
Contain in the monomer (b) of alkoxyl, q is preferably 1～30, is more preferably 2～10, and especially good is 2～5.
In the general formula (II), R is preferably ethylidene or propylidene, and especially good is ethylidene.R in the general formula (II) also can be the combination of two or more alkylidenes.At this moment, being preferably at least one R is ethylidene.The combination of R can be enumerated the combination of ethylidene/propylidene, the combination of ethylidene/butylidene.
The monomer (b) that contains alkoxyl also can be two or more mixture.
The concrete example that contains the monomer (b) of alkoxyl for example can be listed below, but is not limited to these examples.
CH2＝CHCOO-(CH2CH2O)9-H
CH2＝C(CH3)COO-(CH2CH2O)9-H
CH2＝C(CH3)COO-(CH2CH2O)23-H
CH2＝C(CH3)COO-(CH2CH2O)50-H
CH2＝C(CH3)COO-(CH2CH(CH3)O)9-H
CH2＝CHCOO-(CH2CH(CH3)O)9-H
CH2＝C(CH3)COO-(CH2CH(CH3)O)9-H
CH2＝C(CH3)COO-(CH2CH2O)5-(CH2CH(CH3)O)2-H
CH2＝C(CH3)COO-(CH2CH2O)8-(CH2CH(CH3)O)6-H
CH2＝CX1-(CH2CH2O)n-CH3
CH2＝CX1COO-(CH2CH(CH3)O)n-CH3
CH2＝CX1COO-(CH2CH2O)5-(CH2CH(CH3)O)3-CH3
Fluorinated copolymer also can comprise cross-linkable monomer.Cross-linkable monomer can be has at least two reactive groups and/or carbon-to-carbon double bond and not fluorine-containing chemical compound.Cross-linkable monomer can be the chemical compound with at least two carbon-to-carbon double bonds or has the chemical compound of at least one carbon-to-carbon double bond and at least one reactive group.The example of reactive group has: hydroxyl, epoxy radicals, chloromethyl, blocked isocyanate base, carboxyl etc.Among the present invention, do not use to have amino monomer.
Cross-linkable monomer is non-fluorine cross-linkable monomer preferably, is more preferably two (methyl) acrylate.
What cross-linkable monomer was especially good is the chemical compound shown in the general formula (III) (aklylene glycol two (methyl) acrylate);
CH
2＝C(X
3)-C(＝O)-O-(R
1O)
q-C(＝O)-C(X
3)＝CH
2 (III)
In the formula, each X
3Be hydrogen atom or methyl;
R
1The carbon number that can be replaced by hydroxyl for part or all of hydrogen atom is 2～10 alkylidene;
Q is 1～50 integer.In addition, R
1Carbon number be 2～10, for example be preferably 2～6, especially good is 2～4.R
1Be preferably ethylidene.
Constitute each monomeric molecular weight or mol ratio of this fluorinated copolymer by control, can give the dispersibility, moisture-absorbing moisture-keeping ability of the lining characteristic of fluorinated copolymer to powder particle, film forming ability, powder particle etc.The weight average molecular weight of fluorinated copolymer of the present invention can be about 1000～1000000, is preferably about 5000～500000.If above-mentioned weight average molecular weight is less than 1000, the then weak and surface treatment that is not suitable for having effect of the present invention of film forming ability; If above-mentioned weight average molecular weight is greater than 1000000, then not only the dissolubility of polymer is understood variation, and the dispersibility of surface-treated powder can worsen.In addition, this weight average molecular weight is the value of trying to achieve with polystyrene conversion by gel permeation chromatography.
In the fluorinated copolymer, for example when containing 100 weight portion fluorochemical monomers (a), with respect to fluorochemical monomer (a) 100 weight portions, the amount that contains the monomer (b) of alkoxyl can be 10～400 weight portions, be preferably 25～150 weight portions, be more preferably 43～100 weight portions.If the amount of the above-mentioned monomer (b) that contains alkoxyl then can't obtain hydrophilic less than 10 weight portions; If the amount of the above-mentioned monomer (b) that contains alkoxyl is greater than 400 weight portions, then oil repellent can reduce.When containing cross-linkable monomer, the amount of cross-linkable monomer can be below 30 weight portions, for example can be 0.1～20 weight portion, especially 0.5～10 weight portion.If the amount of above-mentioned cross-linkable monomer then can become hard epithelium greater than 30 weight portions, use the sense of touch variation.In addition, employed fluorinated copolymer for example can be opened the method that is disclosed in the 2000-290640 communique by the Japan Patent spy and synthesizes among the present invention, but is not limited to this method.For example, the polymerization of fluorinated copolymer is not particularly limited, and can select various polymerizations such as polymerisation in bulk, polymerisation in solution, emulsion polymerisation, ray polymerization.For example generally select polymerisation in solution with an organic solvent for use or make water or and with the emulsion polymerisation of organic solvent and water.Generally water dilutes after polymerization, or adds emulsifying agent and make itself and water and milkization, makes treatment fluid by this.
Employed surface conditioning agent is preferably solution, emulsion or aerocolloidal form among the present invention.Surface conditioning agent is for example to contain the surface conditioning agent that fluorinated copolymer and medium (for example liquid medium such as organic solvent and water) form.In the surface conditioning agent, the concentration of fluorinated copolymer for example can be 0.01～50 weight %.
To the above-mentioned amount of coating of desiring to carry out the surface-treated powder body according to the chemical composition of desiring to carry out the surface-treated powder body and particle diameter thereof, porously have or not, oil absorption, water absorption, specific surface area and difference, carry out surface-treated powder body 100 weight portions with respect to desiring, the amount of coating of above-mentioned specific fluorinated copolymer is preferably 0.1～40 weight portion.Be more preferably 0.5～35 weight portion.If above-mentioned amount of coating less than above-mentioned scope, then can't obtain enough effects; If above-mentioned amount of coating greater than above-mentioned scope, then not only can produce the coagulation of the powder particle that is caused by polymer, cause the function reduction of surface-treated powder or the effect in cosmetics to become not enough, and have uneconomic tendency.
Among the present invention, just improve by the usability of the surface-treated powder that specific fluorinated copolymer was covered or with the adaptation of skin, the affinity of other composition that is mixed in raising and the cosmetic formulations, and the usability that is mixed with the cosmetics of these surface-treated powders, the viewpoint of effect and cosmetic persistence is finished in cosmetic, for it is showed more effectively, effectively utilize above-mentioned specific fluorinated copolymer and above-mentioned specific fluorinated copolymer other chemical compound in addition to carry out surface treatment, promptly surface conditioning agent also comprises above-mentioned specific fluorinated copolymer other chemical compound in addition compoundly.
Other chemical compound beyond the above-mentioned specific fluorinated copolymer for example is to be selected from fluorochemicals such as perfluoralkyl phosphate, perfluoro polyether phosphate, Perfluoropolyether silanes, perfluoroalkyl silane; organopolysiloxane; alkyl silane; organic titanate; polyolefin, hydrolecithin (comprising its salt), N-acylamino acid (comprising its salt or compositions); acid ester oil, the chemical compound of more than one in fatty acid (comprising its salt) and the dextrin fatty acid ester.
Among the present invention, as carry out the above-mentioned specific fluorinated copolymer of surface-treated other fluorochemical in addition compoundly, can enumerate perfluoralkyl phosphate, perfluoro polyether phosphate, Perfluoropolyether silanes, perfluoroalkyl silane, PFPE modification polyurethanes, PFPE modification acrylate, perfluoroalkyl modified silicone, PFPE modified silicone etc. with specific fluorinated copolymer.
Perfluoralkyl phosphate can use the known chemical compound of following formula (1), and chemical compound is that the carbon number of the Rf in the chemical compound shown in the following formula (1) is the chemical compound below 6 preferably.
[RfC
nH
2nO]
yPO[OM]
3-y (1)
In the formula, Rf represents that carbon number is 1～6 perfluoroalkyl or perfluor oxygen base alkyl, is straight chain shape or branch-like, can be single chain length and also can be compound chain length.N represents 1～12 integer, and y represents 1～3 integer.M represents hydrogen, alkali metal, ammonium or the ammonium that is substituted.
Perfluoro polyether phosphate can use known chemical compound, and chemical compound is the chemical compound shown in the following formula (2) preferably.
[F(CF
2)
3O[CF(CF
3)CF
2O]
mCF(CF
3)C
nH
2nO]
wP(O)(OH)
3-w (2)
Wherein, m represents 0～50 integer, and n represents 1～16 integer, and w is 1 or 2.Phosphoric acid portion can be the form of the alkali metal salt of Na, K etc. or amine salt, ammonium salt.In addition, also can be and utilize phosphoric acid the two terminal-modified forms that form (Fomblin HC/P2-1000: Su Weisu Simon Rex (Solvay Solexis) company).
Perfluoropolyether silanes can use No. 97/07155 communique of WO and Japan Patent spy to open the known chemical compound of being put down in writing in 2008-214229 communique etc.
Perfluoroalkyl silane can use the known chemical compound of following formula (3), and chemical compound is that the carbon number of the Rf in the chemical compound shown in the following formula (3) is the chemical compound below 6 preferably.
(RfC
nH
2n)
aSiX
4-a (3)
In the formula, Rf represents that carbon number is 1～6 perfluoroalkyl or perfluor oxygen base alkyl, is straight chain shape or branch-like, can be single chain length and also can be compound chain length.N represents 1～12 integer, and a represents 1～3 integer.X represents alkoxyl, hydroxyl, amino or halogen atom.
Commercially available perfluoroalkyl silane can be enumerated Dynasylan F-8261 (winning wound Degussa (Evonik Degussa) company) etc.
PFPE modification polyurethanes can be enumerated the commercially available Fomblin AN-5 of Su Weisu Simon Rex company, Fomblin CAT-5 etc.Other fluorochemical that can be used as surface conditioning agent can be enumerated carboxy-modified PFPE, pure modification PFPE, isocyanate-modified PFPE, ester modified PFPE, three fluoro-alkyl dimethyl trimethyl silicane alcoxyl base esters of silicon acis, fluoropropyl polymethyl siloxane (fluoropropyl methicone) etc.
Organopolysiloxane can have functional group also can not have functional group, organopolysiloxane with functional group can be chosen in side chain or have the organopolysiloxane with linear structure of functional group at two terminal or single ends, can enumerate the chemical compound shown in the following formula (4).
(R
5 3SiO)(R
4 2SiO)
m(R
4 2SiO)
n(SiR
5 3) (4)
In the above-mentioned formula (4), R
4Independent mutually, represent that respectively carbon number is 1～4 low alkyl group or hydrogen atom.There is a plurality of R
5All similarly separate, represent that respectively hydrogen atom, hydroxyl and carbon number are any group in 1～4 the lower alkoxy, m and n represent the integer more than 1, m+n is 2～1000 integer.
Organopolysiloxane specifically can be enumerated the commercially available KF99 of chemical industrial company of SHIN-ETSU HANTOTAI, KF9901, X-24-9171 or X-24-9221 etc.Also can use in addition: trimethyl silicane alcoxyl base esters of silicon acis, side chain have the silicone of dimethyl or alkyl, reactive group, acrylic compounds silicone, silicone acrylate etc.The commercially available organopolysiloxane of chemical industrial company of SHIN-ETSU HANTOTAI can use: KF-96 series, KF-9908 (triethoxysilicane alkyl ethyl poly dimethyl silicon alkoxyethyl polydimethylsiloxane) or KF-9909 (triethoxysilicane alkyl ethyl poly dimethyl silicon alkoxyl ethylhexyl polydimethylsiloxane), KP-541, KP-545, KP-575, KP-561, KP-574, KF-7312F, KF-7312J, KF-7312K, KF-9001 etc.; The commercially available organopolysiloxane of DOW CORNING (Dow Corning) company can use: SH1107C, BY11-018, DC593, FA-4001, CM silicone acrylate (Silicone Acrylate), FA-4002ID silicone acrylate (Silicone Acrylate).Also can use in addition: ring-type hydrogenated methyl silicone such as tetrahydrochysene tetramethyl-ring tetrasiloxane, amino modified silicone, carboxy-modified silicone, silicone alkoxyl oligomer, triethoxysilicane alkyl fluorine modified silicone, triethoxy nine methyl five siloxanes, triethoxy triisopropyl disiloxane, triethoxy butyl dimethyl disiloxane etc.
Employed alkyl silane can be selected with R among the present invention
nSiX
4-nStructure is as the alkyl silane of basic framework.Here, R is the alkyl of straight chain shape or branch-like, and X is hydrogen, alkoxyl, amino or halogen atom.The length of alkyl chain can be carbon number 1～18, specifically can enumerate octyltri-ethoxysilane or octadecyltriethoxy silane etc.Also can be the polyether-modified alkoxy silane that intramolecularly is introduced ether in addition.Commercially available product can be enumerated the Z-6341 of Dow Corning Corporation, the Dynasylan4140 of goldschmidt chemical corporation, the KBM-641 of chemical industrial company of SHIN-ETSU HANTOTAI, KBE-13, the Prosil 9202 of Clariant (Clariant) company etc.
Employed organic titanate can be selected with (C among the present invention
nH
2n-1COO)
aTi (OC
mH
2m-1)
bStructure as the organic titanate of basic framework.In addition, in the formula, n represents 1～26 integer, and m represents 1～12 integer, and a and b are respectively 1～3 integer and have the relation of a+b=4.In addition, the alkyl shown in is straight chain shape or branch-like here, and the alkyl that can be single chain length also can be the alkyl of compound chain length.Commercially available organic titanate can be enumerated isopropyl three isostearoyl base titanate esters (Plenact KR-TTS, aginomoto company) etc.
Employed polyolefin can be enumerated the vistanex that has at least one carboxyl in polyethylene, polypropylene etc. and the molecule among the present invention.For example can enumerate with the Japan Patent spy open the known chemical compound put down in writing in the clear 63-179972 communique, be molecular weight be 500～20000 and fusing point be the oxidic polyethylene that obtains of low molecular polyethylene more than 40 ℃ or polypropylene oxidation, maleylation polyethylene, its chlorinated polypropylene etc.
Employed hydrolecithin among the present invention is so long as have the glyceride of phosphate and get final product, and this hydrolecithin can be enumerated iodine number that the natural lecithin that will extract or LYSOLECITHIN SUNLECITHIN A (lysolecithin) and synthetic lecithin hydrogenation form in yolk, Semen sojae atricolor, corn, Semen Allii Tuberosi etc. be hydrolecithin below 15.Employed hydrolecithin also can be the salt form among the present invention, is preferably the water-insoluble hydrolecithin slaine of Al, Mg, Ca, Zn, Zr, Ti etc.Especially good is the hydrolecithin (hydrolecithin that comprises the salt form) with the fusing point more than 50 ℃.For example can enumerate the Japan Patent spy and open clear 60-184571 communique, Japan Patent spy and open the known chemical compound of being put down in writing in clear 60-190705 communique, the special fair 4-58443 communique of Japan Patent, for example the hydrogenated soya phosphatide matter Basi s LS-60HR of the hydrogenation elgen No.5 of industrial group of Asahi Chemical Industry or day company of clear Ao Liao group (Nisshin OilliO Group) etc.Other hydrolecithin with phosphate can be enumerated day commercially available Lipidure series of oily company such as methacryloxyethyl phosphocholine.
Employed acylated amino acid is that carbon number is the satisfied fatty acid below 20 and be selected from aspartic acid (asparaginic acid) more than 12 among the present invention; glutamic acid (glutamic acid); alanine (alanine); lysine (lysine); glycine (glycine); sarcosine (sarcosine); proline (proline); amino acid whose acyl group chemical compound in the hydroxyproline (hydroxyproline); or be derived from Semen Tritici aestivi or Semen Pisi sativi; peptide of plants such as millet (peptide) or silk peptide (silk peptide); be derived from the complete hydrolysis product of the peptide etc. of animal; amino acid whose carboxyl can be free radical, perhaps also can form K; Na; Fe; Zn; Ca; Mg; Al; Zr; the salt of Ti etc.Specifically can enumerate the commercially available Amisoft HS-21P of aginomoto company, Amihope LL (lauroyl lysine) etc., commercially available Soypon SLP, Soypon SCA, the Alanon AMP of (Kawaken Fine Chemicals) company that refine ground in the river, the Sepilift DPHP that France match Bick (Seppic) company is commercially available etc., the Sarcosinate MN that day photochemistry (Nikko Chemicals) company is commercially available etc., Pellicer, Aminofoamer, Aminosurfact, Aminocoat etc. that company of Asahi Chemical Industry is commercially available.These acylated amino acids also can be the form with the compositions of fatty acid.Acyl group lipoamino acid (lipoamino acid) compositions can be enumerated the commercially available Sepifeel One of match BIC Corp (by palmityl proline, palmitoyl sarcosine, palmityl glutamic acid, these 4 kinds compositionss that become branch to constitute of Palmic acid).
Employed acid ester oil is preferably that to comprise total carbon number be that ester compounds more than 16 and acid number are the chemical compound more than 15 among the present invention, and above-mentioned ester compounds can be that 1～36 one or more kinds of alcohol and carbon number are that 1～36 one or more kinds of carboxylic acid reactions obtain by making carbon number.Above-mentioned acid ester oil is that the Japan Patent spy opens the known chemical compound shown in the 2004-51945 communique, specifically can enumerate day clear Ao Liao commercially available Salacos MIS (the different stearyl ester of decanedioic acid), SalacosMOD (Azelaic Acid octyl group dodecyl ester), Salacos 1A (adipic acid octyl group dodecyl ester), the Salacos HD (dimeric dibasic acid octyl group dodecyl ester) etc. of group company.
Can to enumerate carbon number be 12～22 straight chain shape or branch-like is saturated or unsaturated fatty acid to employed fatty acid among the present invention, for example can enumerate fatty acids such as lauric acid, myristic acid, Palmic acid, stearic acid, oleic acid, linolenic acid, palmitoleic acid, behenic acid, the tar acid that holds with both hands with both hands, 2 ethyl hexanoic acid, different tridecanoic acid, different myristic acid, different Palmic acid, isostearic acid, isobehenic acid, the slaine of perhaps above-mentioned fatty acid and Ca, Mg, Zn, Zr, Al, Ti etc.
In addition, as can carry out the surface-treated chemical compound compoundly, can enumerate alkyl phosphoric acid and salt thereof, alkyl carboxylic acid and salt thereof, alkylsurfuric acid and salt thereof, amidosulfonic acid and salt thereof, alkyl ether carboxylic acid and salt thereof, polyoxyethylene alkyl ether phosphoric acid and salt thereof, polyoxyethylene alkyl ether sulphuric acid and salt thereof, methyl-monosilane alcohol/three PEG-8 coconut oil fat acid glycerides and dextrin fatty acid ester etc. with employed specific fluorinated copolymer among the present invention.Commercially available above-claimed cpd has daylight company commercially available Akypo RLM45NV, ECT-3NEX etc., the Monosiliol C that Ai Ximei (Exsymol) company is commercially available etc., but be not limited to these chemical compounds.Can these chemical compounds be handled with the form of combination according to the target effect of surface-treated powder.
Specific fluorinated copolymer (note deals with agent A) and therewith compound proportioning of carrying out other composition of surface-treated (note deals with agent B) are preferably A: B is 39.0～0.1 parts: 0.1～39.0 part; this other composition is for example for being selected from perfluoralkyl phosphate; perfluoro polyether phosphate; Perfluoropolyether silanes; other fluorochemical beyond the above-mentioned fluorinated copolymers such as perfluoroalkyl silane; organopolysiloxane; alkyl silane; organic titanate; polyolefin; hydrolecithin (comprising its salt); N-acylamino acid (comprising its salt or compositions); acid ester oil, the chemical compound of more than one in fatty acid (comprising its salt) and the dextrin fatty acid ester.Be more preferably A: B is 34.5～0.5 parts: 0.5～34.5 part.Proportioning is according to the kind of the kind of powder body or cosmetics and the incorporation in cosmetics and difference, but if surpass above-mentioned ratio, the tendency that then has the effect in cosmetics to reduce.
Employed powder body can be selected spendable powder body in the various fields among the present invention,, when selecting as purposes with cosmetics, can select can be used for the powder body of cosmetics that is.In addition, can select any powder body in inorganic particle and the organic powder.
For example, inorganic particle can be enumerated boron nitride, sericite, natural mica, the calcining Muscovitum, synthetic mica, synthetic sericite, aluminium oxide, Muscovitum, Talcum, Kaolin, bentonite (bentonite), Montmorillonitum (smectite), calcium carbonate, magnesium carbonate, calcium phosphate, silicic acid anhydride, magnesium oxide, stannum oxide, ferrum oxide, yittrium oxide, chromium oxide, titanium oxide, zinc oxide, cerium oxide, aluminium oxide, magnesium oxide, chromic oxide gel, Prussian blue, ultramarine (ultramarine), calcium phosphate, aluminium hydroxide, barium sulfate, magnesium sulfate, silicic acid, Magnesiumaluminumsilicate, calcium silicates, barium silicate, magnesium silicate, aluminium silicate, strontium silicate, carborundum, Afluon (Asta), the wolframic acid slaine, magnesium aluminate, the metasilicic acid magnesium aluminate, the chlorine hydroxy Al, clay (clay), zeolite (zeolite), hydroxyapatite (hydroxyapatite), ceramic powders, spinelle (spinel), mullite (mullite), cordierite (cordierite), aluminium nitride, titanium nitride, silicon nitride, lanthanum, samarium, tantalum, terbium, europium, neodymium, Mn-Zn ferrite (ferrite), the Ni-Zn ferrite, carbonization silicone (silicone carbide), cobalt titanate, Barium metatitanate., iron titanate, the lithium titanate cobalt, cobalt aluminate, contain antimony oxidation tin, the stanniferous Indium sesquioxide., magnetic iron ore (magnetite), aluminium powder, bronze, argentum powder, platinum powder, copper powder, precious metal colloid, iron powder, zinc powder, cobalt blue, cobalt violet, cobalt green, the low price titanium oxide, the micropartical titanium oxide, butterfly-shaped barium sulfate, the petal-shaped zinc oxide, four foot shape zinc oxide, the micropartical zinc oxide; Pearlescent pigment can be enumerated titanium oxide lining Muscovitum, titanium oxide lining Muscovitum, titanium oxide lining synthetic mica, titanium oxide lining silicon dioxide, titanium oxide lining synthetic mica, titanium oxide lining Talcum, zinc oxide lining silicon dioxide, the titanium oxide pearlescent pigments such as painted Muscovitum, colcother lining mica titanium, colcother and black iron oxide lining mica titanium, carmine (carmine) lining mica titanium, Prussian blue lining mica titanium that are covered.Specifically can enumerate Iriodin (registered trade mark) series of Merck (Merck) company, Timiron (registered trade mark) series, Colorona (registered trade mark) series, Dichrona (registered trade mark) series, Xirona (registered trade mark) series, Ronastar (registered trade mark) series, the Desert Reflections series of BASF (BASF) company, Timica series, Flamenco series, Cloizonne series, Duocrome series, Gemtone series, Cellini series, Mearlmaid series, Reflecks series, Chroma-Lite series, Cosmica series, like Prestige (registered trade mark) series of card (Eckart) company, Visionaire (registered trade mark) series, Mirage series, the Metashine of NHTechno company (registered trade mark), Japan's light grinds the Prominence (registered trade mark) of company, the Cosmetica White Pearl series of CQV company, sharon Pearl series etc., the Precioso White Pearlescent Pigments series of forefathers (Taizu) company etc.Can enumerate aluminium flake (flake), the titanium dioxide silicon chip, alumina wafer, the effect pigment of sheet glass etc. (effect pigment), colcother lining Muscovitum, carmine, titanium oxide lining borosilicic acid (sodium/calcium), titanium oxide lining borosilicic acid (calcium/aluminum), Bismuth Oxychloride, guanin, powder of stainless steel, tourmaline (tourmaline) powder, sapphire (sapphire) or ruby gems such as (ruby) pulverized and powder, Fructus Mangifera Indicae purple (Mango Violet), glass fibre, carbon fiber, silicon carbide fibre, alumina fibre, β-wollastonite (β-wollastonite), eakleite (xonotlite), potassium titanate fibre, aluminum borate fiber, the alkali magnesium sulfate fiber, silicon nitride fiber etc.
Organic powder for example can be enumerated metallic soap; the single long acyl basic amino acid of N-; the amidosulfonic acid multivalent metal salt; the succinum powder; white carbon black; tar colorant color lake (lake) changed the powder that forms; the powder that the natural pigment color lakeization is formed; polyamide powder; polyester powder; polyethylene powders; the polyurethanes powder; polypropylene powder; the polystyrene powder; the benzoguanamine powder; polymethyl-benzene and guanamines powder; the polytetrafluoroethylene (PTFE) powder; cellulose powder; silk powder (silk powder); organosilicon powder; divinylbenzene-styrol copolymer; vinylite; Lauxite; phenolic resins; fluororesin; silicones; acrylic resin; melmac; epoxy resin; the powder of synthetic resin such as polycarbonate resin; nylon fiber; the powder body of microcrystalline celluloses such as polyester fiber, starch powder; the CI pigment yellow; CI pigment orange etc.Tar colorant can be enumerated red No. 3, red No. 10, red No. 106, red No. 201, red No. 202, red No. 204, red No. 205, red No. 220, red No. 226, red No. 227, red No. 228, red No. 230, red No. 401, red No. 505, yellow No. 4, yellow No. 5, yellow No. 202, yellow No. 203, yellow No. 204, yellow No. 401, blue No. 1, blue No. 2, blue No. 201, blue No. 404, green No. 3, green No. 201, green No. 204, green No. 205, orange No. 201, orange No. 203, orange No. 204, orange No. 206, orange No. 207 etc.; Natural pigment can be enumerated carmine, laccaic acid (laccaic acid), carthamin (carthamin), brazilin (brazilin), crocin (crocin), chlorophyll (chlorophyll), the beta-carotene (powder body of natural pigment such as β-carotin), Flos Carthami (safflower) powder etc.The shape of powder body can be Powdered also can be fibrous.When selecting cosmetics, as long as in the scope of particle diameter about 1nm～2000 μ m, can mix cosmetics and get final product as purposes.
In addition, among the present invention, above-mentioned powder body (carrying out surface treatment powder body before) also can be the powder body that two or more compoundization are formed.For example can be set forth in the powder body (Excel Mica JP-2 or Excel Pearl: three change into limited company well) that Muscovitum or pearlescent pigment particle surface form compoundization of aluminium hydroxide, the powder body (Powder La Vie: three change into limited company well) that hydroxyl phosphorus Calx and compoundization of zinc oxide is formed on sericite or pearlescent pigment surface, micropartical titanium oxide and micropartical zinc oxide disperseed the powder body (TZ-Powder Type well changes at 1: three) that mixes, with Talcum and fine zinc white, the powder body (TZ-Powder Type well changes into limited company at 2: three) that the dispersion of micropartical titanium oxide mixes, the mixture of Dimethicone/Vinyl Dimethicone and silicon dioxide (DOW CORNING 9701 Cosmetic Powder), the mixture of Dimethicone/Vinyl Dimethicone and titanium oxide (DOW CORNING EP-9261 TI Cosmetic Powder), the mixture of Dimethicone/Vinyl Dimethicone and aluminium oxide (DOW CORNING EP-9293 AL Cosmetic Powder), the mixture of Dimethicone/Vinyl Dimethicone and lauroyl lysine (DOW CORNING EP-9289 LL Cosmetic Powder), day waves catalyst and changes into the commercially available Coverleaf series of industrial group, Concelight series etc.
In addition, for desiring to carry out the surface-treated powder body among the present invention, in order to promote affinity or the anchorage with surface conditioning agent, also can utilize at least a oxide or hydrous oxide in for example aluminum, calcium, magnesium, cerium, silicon, zirconium, titanium, zinc, ferrum, cobalt, manganese, nickel and the stannum to be covered in advance.These chemical compounds can be used to carry out the surface-treated surface conditioning agent in utilizing the present invention carries out being covered in advance before the surface treatment, also can be covered when surface treatment.In addition, the particle of can be covered this oxide or hydrous oxide also can make it carry out separating out on the surface-treated powder particle surface desiring.The amount of coating of these the 3rd materials is preferably for utilizing surface-treated powder to make the function of fluorochemical of the present invention necessary minimum for being embodied.
Among the present invention, there is no particular restriction for the method for the surface conditioning agent that is covered on powder body, especially specific fluorinated copolymer, can implement by known method.Surface treatment method roughly is divided into dry process and damp process.For example use Henschel mixer (Henschel mixer) or ball mill (ball mill), jet mill (jet mill), kneader (kneader), planetary-type mixer (planetary mixer), minitype vertical type blender (pony mixer), sand mill (sand mill), super micron mill (attritor), ribbon mixer (ribbon blender), disperse mixer (disper mixer), homomixer (homomixer), extruder blender or pulverizers such as (extruder), mixer, dispersion machine, employed surface conditioning agent and powder body are mixed contact certain hour, handle by this.At this moment, also can simultaneously apply mechanochemistry (mechanochemical) property mechanical force, plasma (plasma), flame, ultraviolet, electron beam, superheated vapour, laser, electromagnetic wave homenergic, one side is handled.Damp process is to make powder body and surface conditioning agent be dispersed in water or solvent, supercritical fluid (water, CO
2Deng) in and make it mix contact, make solvent evaporation then, can handle by this.
In addition; employed specific fluorinated copolymer among the present invention is selected from perfluoralkyl phosphate with comprising; perfluoro polyether phosphate; Perfluoropolyether silanes; fluorochemicals such as perfluoroalkyl silane; organopolysiloxane; alkyl silane; organic titanate; polyolefin; hydrolecithin (comprising its salt); N-acylamino acid (comprising its salt or compositions); acid ester oil; when the chemical compound of more than one in fatty acid (comprising its salt) and the dextrin fatty acid ester carries out surface treatment compoundly; with only to utilize above-mentioned specific fluorinated copolymer to carry out the surface-treated situation same, also can carry out surface treatment by making powder body mix to contact with the surface conditioning agent that also comprises above-claimed cpd.In addition, according to selecting best lining manufacture method to get final product, be not subjected to the qualification of manufacture method especially for the kind of the character of carrying out the chemical compound that surface treatment selects (aqueous, solid, shaped, gel etc.), rerum natura (fusing point, boiling point, vitrification point, dissolubility, reactivity etc.) and the powder body desiring to be covered compoundly.
When carrying out surface treatment, can enumerate following method compoundly: after specific fluorinated copolymer is handled in lining earlier, the method for other surface conditioning agent composition beyond this specific fluorinated copolymer that is covered again; The method of specific fluorinated copolymer and this specific fluorinated copolymer other surface conditioning agent composition in addition simultaneously is covered; Behind other surface conditioning agent composition beyond the specific fluorinated copolymer of lining, the method for specific fluorinated copolymer etc. again is covered earlier.
Coating method is following method preferably: only utilizing above-mentioned specific fluorinated copolymer to carry out under surface-treated situation and compound any situation of carrying out in the surface-treated situation, with the powder particle desiring to be covered in advance in air or in the liquid or with the condition of other powder body coexistence under be covered again after disperseing, perhaps be covered simultaneously.
Therefore specific fluorinated copolymer of the present invention if only the oil repellent group is exposed from the powder particle surface, then can show water and oil repellant owing to have oil repellent group and hydrophilic radical in its molecule.For the affinity or the dispersibility of the excellence of other composition of being mixed in the surface-treated powder that obtains to have oil repellent and the cosmetic formulations, hydrophilic oil repellent is favourable.Specific fluorinated copolymer of the present invention can expose oil repellent group and hydrophilic radical simultaneously according to coating method or amount of coating on the powder particle surface, show hydrophilic oil repellent by this.
About obtaining the coating method of hydrophilic oil repellent,, then can obtain hydrophilic oil repellent surface-treated powder if to carry out surface treatment than the higher amount of coating of amount of coating that can in the operation that is covered together, obtain water and oil repellant.Employed specific fluorinated copolymer is by having introduced the poly alkylene glycol of optimised quantity among the present invention in molecule, and therefore hydrogen bond force or the epithelium with the powder body base material forms the power height, is easy to handle; At this moment, if less, then show water and oil repellant to the amount of coating of powder particle, but if amount of coating increases, it is superfluous that then free polyalkylene glycol chain becomes, and because of the mobility (mobility) of the residing environment of powder particle by molecule contacts with water, thereby shows hydrophilic.In addition, method of temperature in the time of also can becoming method that acidity or alkalescence handles or control treatment by the pH that makes powder body when the surface treatment etc., also can be after utilizing existing fluorochemical to be covered, utilize specific fluorinated copolymer of the present invention to be covered again, thereby obtain hydrophilic oil repellent, but according to the kind of powder body and different.
Another coating method that obtains hydrophilic oil repellent is repeatedly to be covered to obtain hydrophilic oil repellent.That is, will utilize specific fluorinated copolymer to be covered and the surface-treated powder of giving water and oil repellant further is covered with identical or different specific fluorinated copolymers, obtain hydrophilic oil repellent by this.If make the most surperficial expose of fluorine chain at the fast processing layer of the surface-treated powder particle that shows water and oil repellant, and then should be surface-coated, be covered with the fluorine chain of the polymer of second processing layer and the fluorine chain mode in opposite directions of fast processing layer by this, then polyalkylene glycol chain can be in particle the most surperficial exposing and show hydrophilic oil repellent.Also can operate and control hydrophilic oil repellent and water and oil repellant by carrying out this repeatedly.
The evaluation methodology of water and oil repellant and hydrophilic oil repellent can be adopted the method for the contact angle of mensuration and water or squalane (squalane).According to this method, the contact angle that the water and oil repellant of surface-treated powder of the present invention is preferably with water or squalane is more than 80 °.The hydrophilic oil repellent of surface-treated powder of the present invention be preferably contact angle with water be below 20 ° and with the contact angle of squalane be more than 80 °, be more preferably contact angle with water and be below 10 ° and with the contact angle of squalane be more than 100 °.
The contact angle of these surface-treated powders and squalane be meant with powder filled to metalware and the pressure that applies 6MPa form squalane drop that on the profiled surface of this powder body, drips and powder surface angulation 10 seconds.This angle is big more, and the effect of then repelling this drop is high more, shows liquid repellency more; This angle is more little, then shows lyophily more.
Hydrophilic other evaluation methodology can be adopted following method: add entry in beaker, drop into a spot of powder body, utilize spatula (spatula) to stir after 50 times, observe buoyant powder body and the state that is dispersed in the powder body in the water layer on the water surface with the frequency of per second 2 times.Surface-treated powder with hydrophilic oil repellent of the present invention is in that almost not have powder body on the water surface floating and be dispersed with powder body in water layer.
Contain cosmetics by the powder body that chemical compound was covered that comprises specific fluorinated copolymer of the present invention at least with hydrophilic oil repellent, compare with the cosmetics that contain existing fluorochemical processing powder body, with the affinity excellence of other composition that is mixed in the cosmetic formulations, therefore the usability in cosmetics, make up and finish excellence aspect effect, cosmetic persistence and the quality stability.
In the water compositions such as polyhydric alcohol that surface-treated powder of the present invention can be dispersed in the cosmetic formulations by showing hydrophilic oil repellent to be mixed.This dispersion liquid is coated on the skin, and the filming of surface-treated powder after the water composition volatilization shows oil repellent.This just mean can improve the existing surface-treated powder that shows water and oil repellant to the dissolubility of the oiliness composition of cosmetics or water composition or emulsibility, bad dispersibility and with the situation of the adaptation difference of skin.By the present invention, can solve the problem that the accommodation of the preparation that is mixed with the powder body of handling through existing fluorochemical is restricted.As an example, can realize mixing and make preparation integral body become the design of water and oil repellant in the oiliness composition by the composition that the surface-treated powder that this is shown hydrophilic oil repellent mixed in the water composition and will show water repellency, thus can realize having than in the past better the preparationization of function or with the preparationization of different in the past novelty.
The surface-treated powder that the present invention obtained can mix unification kind or two or more in cosmetics.
(cosmetics of the present invention)
Cosmetics of the present invention are the cosmetics that contain above-mentioned surface-treated powder.That is, this surface-treated powder can be prepared by said method.
Among the present invention, the prescription of cosmetics there is no especially difficulty, can be based on employed technology in the past, especially surface-treated powder is mixed technology in the cosmetics (for example emulsifying etc.) and obtain the target cosmetics.
When mixing surface-treated powder of the present invention in the cosmetics, its incorporation is according to the kind of cosmetics and dosage form and difference is preferably 0.1～100 weight % in cosmetics are all formed.In addition, surface-treated powder of the present invention can form the dispersion with water composition, and when mixing in the cosmetics, its incorporation is not particularly limited.
Other composition that is mixed in the cosmetics of the present invention for example can be enumerated oiliness composition, water composition and surfactant.
But oiliness composition illustration: safflower oil; soybean oil; Radix Oenotherae erythrosepalae oil; Oleum Vitis viniferae; Rosehips oil (rose hip oil); Hawaii drupe oil (kukui nut oil); almond oil (almond oil); Oleum sesami; Semen Tritici aestivi germ oil; Semen Maydis oil; Oleum Gossypii semen; American Avocado Tree oil (avocado oil); olive oil; Chinese toon oil; peach kernel oil; Oleum Ricini; Oleum Arachidis hypogaeae semen; hazelnut oil (hazelnut oil); macadimia nut oil (macadamia nut oil); Bai Manghua seed oil; cocoa butter; Adeps Bovis seu Bubali resin (shea butter); haze tallow; cocos nucifera oil; Petiolus Trachycarpi oil; palm-kernel oil; Adeps Bovis seu Bubali; house oil; ermine oil; butter; elgen; Oleum Testudinis oils such as (turtle oil); Cera Flava; spermaceti; lanoline (lanolin); Brazil wax (carnauba wax); candelilla wax (candelilla wax); Simmondsia chinensis oil wax classes such as (jojoba oil); liquid paraffin (liquid paraffin); the different paraffin of liquid; squalane; Squalene; vaseline; paraffin; ceresine (ceresin); microwax (microcrystalline wax); hydro carbons such as alpha-olefin oligomer; lauric acid; myristic acid; Palmic acid; stearic acid behenic acid; oleic acid; linolenic acid; 9-undecylenic acid; hydroxy stearic acid; fatty acids such as lanolin fatty acid; myristyl alcohol; spermol; cetearyl alcohol; stearyl alcohol; aralkyl alcohol behenyl alcohol; oleyl alcohol; the Simmondsin. another name for; batilol (batyl alcohol); cholesterol (cholesterol); plant sterol (phytosterol); lanolin alcohol; senior alcohols such as isooctadecanol; cholesterol; sitosterol (sitosterol); plant sterol; sterols such as lanosterol; ethyl oleate; isopropyl myristate; Octanoic acid, hexadecyl ester; malic acid two different stearyl esters; esters such as tricaprylin; dimethyl polysiloxane; methyl phenyl silicone; alkyl-modified silicone; ring-type silicone pentamer; ring-type silicone hexamer; methyl gathers trimethicone; the caprylyl polymethyl siloxane; poly-di-ethyl siloxane; poly-trimethicone; the alkyl polymethyl siloxane; the tocopherol trisiloxanes; silicones such as fluorine carbon silicone; perfluoro polyether oil; perfluocarbon; fluorine such as hydrogen fluorine ether are oil preparation, ethyl acetate; butyl acetate; organic solvents such as toluene etc.
Water composition has: ethanol, lower alcohols such as isopropyl alcohol, 1, the 3-butanediol, propylene glycol, Polyethylene Glycol, glycerol, diglycerol, polyglycereol, trehalose (trehalose), erithritol (erythritol), mannitol (mannitol), xylitol (xylitol), Sorbitol (sorbitol), maltose polyhydric alcohol such as (maltose), and arabic gum (arabic gum), Tragacanth (tragacanth), galactan candy (galactan), tragon (carob gum), guar gum (guar gum), karaya (karaya gum), carrageenin (carrageenan), pectin (pectin), agar (agar) Fructus cydoniae oblongae seed (quince seed) (marmelo Cydonia oblonga), starch (rice, corn, Rhizoma Solani tuber osi, Semen Tritici aestivi), dextrin, glucosan (dextran), alginate jelly (algae colloid), Te Lantuo glue, locust bean gum department of botany's water soluble polymers such as (locust bean gum), Xanthan gum (xanthan gum), glucosan, succinoglycan (succinoglucan), pulullan polysaccharide department of microbiology water soluble polymers such as (pullulan), collagen protein (collagen), casein (casein), albumin (albumin), gelatin animals such as (gelatin) is a water soluble polymer, carboxymethyl starch, starch such as methyl hydroxypropyl starch are water soluble polymer, methylcellulose, ethyl cellulose, methylhydroxypropylcellulose, carboxymethyl cellulose, hydroxy methocel, hydroxypropyl cellulose, NC Nitroncellulose, cellulose sodium sulfate, sodium carboxymethyl cellulose, crystalline cellulose, the cellulose-based water soluble polymer of cellulose powder esters, sodium alginate, alginic acid such as propylene glycol alginate are water soluble polymer, polyvinyl methyl ether, ethylene base system water soluble polymers such as CVP Carbopol ETD2050, polyoxyethylene is a water soluble polymer, polyoxyethylene-polyoxypropylene copolymerization system water soluble polymer, sodium polyacrylate, polyethyl acrylate, acrylic acid series water soluble polymers such as polyacrylamide, polymine, other synthesizing water-solubility macromolecule such as cationic polymer, bentonite, Magnesiumaluminumsilicate, Montmorillonitum (montmorillonite), beidellite (beidellite), nontronite (nontronite), saponite (saponite), Strese Hofmann's hectorite. (hectorite), silicic acid anhydrides etc. are inorganic to be water soluble polymer etc.In addition, these water soluble polymers also comprise epitheliums formation agent such as polyvinyl alcohol or polyvinyl pyrrolidone.
Surfactant can be enumerated: the anionic surfactant, and it comprises fatty acid soaps such as sodium stearate or Palmic acid triethanolamine, alkyl ether carboxylic acid and salt thereof, the condensation substance salt of aminoacid and fatty acid, alkyl sulfonate, alkene sulfonate, the sulfonate of fatty acid ester, the sulfonate of fatty acid amide, formaldehyde condensation is a sulfonate, alkyl sulfate salt, second level higher alcohol sulfate salt, alkyl and allyl ether sulfuric acid, the sulfuric acid of fatty acid ester, the sulfuric acid of fatty acid alkanol amides, the sulfuric ester salt of turkey red oil (turkey red oil) etc., alkylphosphonic, ether phosphate, alkyl allyl ether phosphate, amidophosphoric acid salt, the N-acylamino acid is an activating agent etc.; Cationic surfactant, it comprises the amine salt of alkylamine salt, polyamine and amino alcohol fatty acid derivatives etc., alkyl quaternary ammonium salts, aromatic series quaternary ammonium salt, pyridine
Salt, imidazoles
Salt etc.; Nonionic surfactant, it comprises sorbitan fatty acid ester, fatty acid glyceride, polyglyceryl fatty acid ester, methyl glycol fatty acid ester, cithrol, sucrose fatty acid ester, polyoxyethylene alkyl ether, the polyoxypropylene alkyl ether, polyoxyethylene alkyl phenyl ether, polyoxyethylene fatty acid ester, polyoxyethylene sorbitan fatty acid ester, the polyoxyethylene sorbitol fatty acid ester, the polyoxyethylene fatty acid glyceride, the polyoxyethylene methyl glycol fatty acid ester, polyoxyethylene castor oil, polyoxyethylene hardened castor oil, polyoxyethylene phytostanol ether, polyoxyethylene plant sterol ether, polyoxyethylene beta-cholestanol ether, the polyoxyethylene cholesterol ethers, polyoxyalkylene modification organopolysiloxane, polyoxyalkylene/alkyl co-modified organopolysiloxane, polyglycerol-modified organopolysiloxane, alkanolamide, sugar ether, sugar amide etc.; And amphoteric surfactant, it comprises betanin, aminocarboxylate, imidazolidine derivatives etc.
In the cosmetics of the present invention, effect of the present invention can not diminished, it is usability, effect is finished in cosmetic, the cosmetic persistence, affinity and quality stability with the excellence of other composition that is mixed in the cosmetic formulations, safety to organism, in the scope to environmentAL safety etc., suitably mix employed other composition, for example pigment dispersing agent in cosmetics etc. usually, oil preparation, surfactant, UV absorbent, antiseptic, antioxidant, epithelium forms agent, wetting agent, thickening agent, dyestuff, pigment, various medicament (vitaminss, astaxanthin (astaxanthin), alpha-lipoic acid (α-lipoic acid), coenzyme Q10 (coenzyme Q10) etc.), spice etc.
Dosage form to cosmetics of the present invention is not particularly limited.The dosage form of cosmetics for example can be selected: existing known dosage forms such as emulsion form, white shape, solid shape, pasty state, gel, Powdered, multilamellar shape, Mu Sizhuan and spray form.Particularly, cream base (makeup base) before the cosmetic cosmetics can be enumerated and make up, muffin (powder foundation), foundation emulsion (liquid foundation), the oiliness foundation cream, bean noodles (stick foundation), compression muffin (pressed powder), honey powder (face powder), white lead, lipstick, lip coat, lip gloss (lip gloss), concealer (concealer), rouge, eye shadow (eye shadow), eyebrow pencil (eyebrow pencil), eye-liner (eyeliner), mascara (mascara), water-based nail polish (nail enamel), the oiliness nial polish, the oil-in-water type nial polish, armor face oil (enamel top coat), oil at the bottom of the armor (enamel base coat) etc.; The skin care cosmetics can be enumerated emollient cream (emollient cream), cold cream (cold cream), skin whitener, emulsion, astringent, beautifying liquid, facial film, sebum conditioning and reveal (carmine lotion), facial cleanser, foam cleansing milk, the frost of washing one's face, the granule of washing one's face, makeup removing material (make cleansing), body shaping breast (body gloss), anti-Exposure to Sunlight or Exposure to Sunlight with uvioresistant cosmetics such as frost or emulsion etc.; Cosmetic hair can be enumerated hair care honey (hair gloss), suppurative mastitis (hair cream), shampoo (hair shampoo), hair care agent (hair rinse), hair dye (hair coloring), detanglers (hair brushing) etc.; The hidroschesis cosmetics can be enumerated frost or emulsion, powder, mist agent, walk the fragrant atmosphere goods of pearl type hidroschesis etc.; Other cosmetics can be enumerated emulsion, soap, bath shampoo, perfume etc.
(purposes beyond the cosmetics)
The above-mentioned surface-treated powder of putting down in writing (surface-treated powder of the present invention) not only can be applicable to cosmetics, and various fields such as the powder body filler that also can be applicable in ink, coating, resin concentrates, the paper etc. to be mixed, ceramic material, magnetic material, rare earth, optical material, conductive material, voltage material.Especially use in other field when can be used for the powder body of cosmetics, surface-treated powder illustrated in the above-mentioned cosmetic use also can similarly adopt in this other field.
Below, the present invention is described in detail to enumerate embodiment and comparative example, but the present invention is not limited to these embodiment.
[embodiment]
[Production Example 1-1～1-3]
List the Production Example of employed fluorinated copolymer chemical compound among the present invention as follows.
[Production Example 1-1]
Take into account the fluorochemical monomer CH of the 18.6g that packs in the 100ml four-hole boiling flask of agitating device to possessing reflux cooling pipe, nitrogen ingress pipe, temperature
2=CHC (=O) O-CH
2CH
2C
6F
13The polyethylene glycol acrylate CH of (below be designated as C6SFA (a)), 11.4g
2=CHC (=O) O-(CH
2CH
2O)
nThe 2 mercapto ethanol of-H (Blemmer AE90, a day oily limited company makes, the meansigma methods of n is 2, below is designated as AE90 (b)), 0.3g and the methyl ethyl ketone of 45g (below be designated as MEK) carry out nitrogen foaming in 30 minutes.After under nitrogen current, interior temperature being warming up to 50～65 ℃, add the Perbutyl PV (below be designated as PV) of 0.4g, 60～65 ℃ of reactions 6 hours down.Then the solution that is obtained is distilled under about 70 ℃ under reduced pressure and remove MEK, after obtaining faint yellow polymer residue, add the water of 122.4g, after 80 ℃ of following maintenances of interior Wen Zaiyue are more than 1 hour, cool off, make the aqueous dispersions that solid component concentration is about 20 weight %.
[Production Example 1-2]
AE90 among the Production Example 1-1 (b) is replaced with polyethylene glycol methacrylate-styrene polymer CH
2=C (CH
3) C (=O) O-(CH
2CH
2O)
n-H (Blemmer PE350, a day oily limited company makes, the meansigma methods of n is 8, below is designated as PE350 (b)), carry out the polyreaction identical with Production Example 1-1, make the aqueous dispersions that solid component concentration is about 20 weight %.
[Production Example 1-3]
Take into account AE90 (b), the polyethylene glycol acrylate CH of 5.7g of C6SFA (a), the 5.7g of the 18.6g that packs in the 100ml four-hole boiling flask of agitating device to possessing reflux cooling pipe, nitrogen ingress pipe, temperature
2=CHC (=O) O-(CH
2CH
2O)
n-H (Blemmer AE200, day oily limited company makes, and the meansigma methods of n is 4.5, below is designated as AE200 (b)), the 2 mercapto ethanol of 0.3g and the MEK of 45g, carry out the polyreaction identical, make the aqueous dispersions that solid component concentration is about 20 weight % with Production Example 1-1.
[Production Example 1-4]
Take into account AE350 (b), the polyethyleneglycol diacrylate CH of 0.9g of C6SFA (a), the 10.5g of the 18.6g that packs in the 100ml four-hole boiling flask of agitating device to possessing reflux cooling pipe, nitrogen ingress pipe, temperature
2=CHC (=O) O-(CH
2CH
2O)
n-C (=O) CH=CH
2(Blemmer ADE300, a day oily limited company makes, the meansigma methods of n is 7), the lauryl mercaptan of 0.3g and the isopropyl alcohol of 45g carry out the polyreaction identical with embodiment 1, make the aqueous dispersions that solid component concentration is about 20 weight %.
Table 1-1
[embodiment 1-1～1-14 and comparative example 1-1～1-14]
(a1)～(c1) be each fluorinated copolymer used in the present invention, (d1) copolymer shown in is the chemical compound of existing (comparative example) with the perfluoralkyl phosphate (e1).Make and carried out the surface-treated powder body, and each rerum natura of these surface-treated powders is estimated with above-mentioned each chemical compound.List the manufacturing embodiment of surface-treated powder and assessment item and method as follows.
(embodiment 1-1 and comparative example 1-1)
In the sericite FSE of 100g (the three letter miner companies) high-speed mixer of packing into, add mixed solution (50: the 50 weight %) 50g that counts each fluorochemical shown in the table 1 of 3g and IPA (isopropyl alcohol) and water with solid constituent, mixed 30 minutes.To mix thing at 80 ℃ down after dry 3 hours, so 110 ℃ dry 10 hours down.Carry out micronizing then, obtain each fluorochemical and handle sericite.
(embodiment 1-2 and comparative example 1-2)
Employed sericite among embodiment 1-1 and the comparative example 1-1 is replaced with Muscovitum Y-2300 (mountain pass Muscovitum company), similarly carry out surface treatment, obtain each fluorochemical and handle Muscovitum with embodiment 1-1 and comparative example 1-1.
(embodiment 1-3 and comparative example 1-3)
Employed sericite among embodiment 1-1 and the comparative example 1-1 is replaced with Talcum JA-46R (shallow field powder process company), and use with solid component meter and be respectively each the fluorochemical/perfluoralkyl phosphate [CF shown in the table 1-1 of 5g/2g
3(CF
3)
5CH
2CH
2O]
2P (O) OH similarly carries out surface treatment as inorganic agent with embodiment 1-1 and comparative example 1-1, obtains the Combined Processing Talcum of each fluorochemical and perfluoralkyl phosphate.
(embodiment 1-4 and comparative example 1-4)
After will counting the IPA dilution of each fluorochemical of 5g with solid constituent, be added among the titanium CR-50 (the former industry of stone company) of 100g with 10ml.Utilize mixer to mix after 15 minutes, import 250 ℃ superheated vapour, the moment that reaches 200 ℃ in mixer stops to stir, and obtains each fluorochemical and handles powder body.
(embodiment 1-5～1-7 and comparative example 1-5～1-7)
The sericite of embodiment 1-1 and comparative example 1-1 is replaced with yellow LL-100P (titanium industrial group), red R-516PS (titanium industrial group), black BL-100P (titanium industrial group) respectively, similarly carry out surface treatment with embodiment 1-1 and comparative example 1-1, obtain each fluorochemical and handle powder body.
(embodiment 1-8 and comparative example 1-8)
Micropartical titanium oxide (MT-100TV: kingdom's chemical industry (Tayca) company) drop in the deionized water of 1500ml, each fluorochemical of counting 5g with solid constituent is added with the IPA dilution back of 500ml with 100g.Utilize sand mill (the zirconium oxide Rong Qi ﹠amp of DYNO-Mill:1.4L; Blade, the zirconium oxide bead of 0.5mm φ, filling rate are 85%) disperse by 15 minutes circulations.This dispersion liquid under agitation is heated to 80 ℃, drips the 10%HCl aqueous solution and pH is adjusted to 4.5.After dewatering by centrifugalize, 120 ℃ dry 16 hours down, utilize the JET super micron mill to pulverize, obtain each fluorochemical and handle micropartical titanium oxide.
(embodiment 1-9 and comparative example 1-9)
The solid constituent of each fluorochemical of embodiment 1-8 and comparative example 1-8 is made as 8g, and the method for making by shown in embodiment 1-1 and the comparative example 1-1 only adopts IPA solution to carry out surface treatment as solvent, obtains each fluorochemical and handles micropartical titanium oxide.
(embodiment 1-10 and comparative example 1-10)
Handle powder body at each fluorochemical that embodiment 1-8 and comparative example 1-8 are obtained, with employed solvent replacing in the method for embodiment 1-1 and comparative example 1-1 is HFE, and the solid constituent with respect to powder body that will show each fluorochemical shown in the 1-1 is made as 1%, similarly carry out surface treatment with embodiment 1-1 and comparative example 1-1, obtain the dual lining surface treatment micropartical titanium oxide of each fluorochemical.
(embodiment 1-11 and comparative example 1-11)
Chemical company of kingdom), the degree of polymerization in that single end has a triethoxy of each fluorochemical shown in the 5g table 1-1 and 3g is to add the HFE (hydrogen fluorine ether) of 15g and the IPA of 50g in 15 the straight chain shape dimethyl polysiloxane, utilizes kneader to mix 30 minutes to the micropartical zinc oxide of 100g (MZ-300:.After the deionized water that adds 10g again mixed 30 minutes, carry out the JET micronizing after dry 16 hours down, obtain the Combined Processing micropartical zinc oxide of each fluorochemical and silicone at 105 ℃.
(embodiment 1-12 and comparative example 1-12)
Pearlescent pigment (Flamencogold: Engelhardt (Engelhardt) company) be added in the deionized water of 1000ml, add N-stearyl disodium glutamate (the aginomoto company: Amisoft HS-21P) dissolve dispersion of 1.5g again with 100g.Add each fluorochemical shown in the 3g table 1-1 again and heat, utilize kneader to mix 30 minutes to 80 ℃.Drying is 8 hours under 130 ℃, obtains the Combined Processing pearlescent pigment of each fluorochemical processing and acylated amino acid.
(embodiment 1-13 and comparative example 1-13)
To the Amihope of 100g LL (lauroyl lysine: the mixed liquor that adds IPA/HFE=15g/10g aginomoto company), and each fluorine-containing inorganic agent shown in the adding 3g table 1-1, similarly carry out surface treatment with the method for embodiment 1-12 and comparative example 1-12, obtain each fluorochemical and handle AmihopeLL.
(embodiment 1-14 and comparative example 1-14)
The redness No. 202 (changing into company the sixth of the twelve Earthly Branches in the last of the ten Heavenly stems) of 100g is added in the mixed solution of IPA/HFE/ deionized water=40g/15g/100g, one side utilizes propeller-type mixer to stir, and one side utilizes Soniprep (Japanese Waja (Siber Hegner) company) to disperse.After the IPA of each fluorine-containing inorganic agent shown in the Dropwise 5 g table 1-1 and 5g carries out ripening, by the heating in vacuum distillation remove desolvate and 105 ℃ dry down, pulverized 16 hours, obtain each fluorochemical and handle redness No. 202.
The guide look of embodiment 1-1～1-14 and comparative example 1-1～1-14 is shown in table 1-2.
The guide look of table 1-2: embodiment and comparative example
(the contact angle test of water and squalane)
Double faced adhesive tape is attached on the microscope slide, and utilizes powder puff on the another side of double faced adhesive tape, to be coated with each surface-treated powder, till the adhesive tape face loses cohesiveness.The contact angle meter (CA-D) that utilizes consonance interface science company to make drips water or squalane (dripping quantity is 10 μ l) on the powder body coating surface, measure drop and powder body coated face angulation (contact angle) after 20 seconds.(the n number is made as 5)
(usability and fitness test)
By 15 sensory test persons that can carry out the sensory test of surface-treated powder, estimate the usability and the adaptation of each surface-treated powder at same powder body.Evaluation methodology is by to refer to that abdomen rubs, and perhaps coats fingernail or upper arm parts and carries out.Evaluation is undertaken by each sensory test person's absolute evaluation, and its scoring is as follows.◎: very good, zero: good, △: common, *: poor.
(water repellency and hydrophilic evaluation methodology)
The purified water that in the glass beaker of 100cc, adds about 50cc.On the water surface, drop into the processing powder body of about 0.1g, utilize spatula with each second about 2 times frequency stir.Estimate the muddy degree that stirs the water after 50 times, 100 times, 150 times with 5 grades.
＜metewand 〉
5 waters are not seen muddiness.(water repellency is strong)
4 waters are seen muddiness slightly.
3 waters are visible significantly muddy.
2 most of powder body are transferred to aqueous phase.
1 whole powder body are transferred to aqueous phase.(hydrophilic is strong)
(evaluation result)
The evaluation guide look of the surface-treated powder of embodiment 1-1～1-14 and comparative example 1-1～1-14 is shown in table 1-3～table 1-5.
Table 1-3: the contact angle result of the test of water/squalane
| Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) | |
| Sericite FSE | 135°/130° | 133°/133° | 140°/130° | 124°/120° | 141°/135° |
| Muscovitum Y-2300 | 138°/130° | 132°/130° | 137°/133° | 126°/129° | 145°/137° |
| Talcum JA-46R | 134°/127° | 130°/125° | 136°/130° | 126°/129° | 147°/130° |
| Titanium CR-50 | 130°/130° | 132°/133° | 135°/130° | 136°/139° | 146°/139° |
| Yellow LL-100P | 137°/130° | 133°/131° | 138°/132° | 136°/120° | 145°/135° |
| Red R-516PS | 136°/130° | 135°/123° | 135°/128° | 136°/130° | 145°/130° |
| Black BL-100P | 130°/132° | 132°/134° | 133°/130° | 136°/130° | 142°/131° |
| The micropartical titanium oxide | 132°/130° | 132°/133° | 137°/124° | 136°/131° | 145°/130° |
| The micropartical titanium oxide | 8°/130° | 10°/132° | 10°/133° | 136°/130° | 145°/140° |
| The micropartical titanium oxide | 9°/130° | 12°/133° | 8°/130° | 136°/138° | 143°/141° |
| The micropartical zinc oxide | 130°/131° | 132°/130° | 130°/132° | 136°/130° | 145°/130° |
| Pearlescent pigment | 133°/130° | 132°/133° | 139°/131° | 136°/137° | 144°/130° |
| Amihope?LL | 10°/125° | 13°/135° | 10°/128° | 136°/133° | 145°/131° |
| Red No. 202 | 135°/130° | 132°/133° | 140°/133° | 136°/131° | 144°/136° |
Table 1-4: usability/fitness test result
| Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) | |
| Sericite FSE | ○/◎ | ○/◎ | ○/◎ | △/△ | ×/× |
| Muscovitum Y-2300 | ○/◎ | ○/◎ | ○/◎ | △/△ | ×/× |
| Talcum JA-46R | ◎/◎ | ◎/◎ | ◎/◎ | ○/× | △/× |
| Titanium CR-50 | ○/◎ | ○/◎ | ○/◎ | △/× | ×/× |
| Yellow LL-100P | ○/◎ | ○/◎ | ○/◎ | △/× | ×/× |
| Red R-516PS | ○/◎ | ○/◎ | ○/◎ | △/× | ×/× |
| Black BL-100P | ○/◎ | ○/◎ | ○/◎ | △/× | ×/× |
| The micropartical titanium oxide | ○/◎ | ○/◎ | ○/◎ | ○/△ | ×/× |
| The micropartical titanium oxide | ◎/◎ | ◎/◎ | ◎/◎ | ○/× | △/× |
| The micropartical titanium oxide | ◎/◎ | ◎/◎ | ◎/◎ | ○/× | △/× |
| The micropartical zinc oxide | ○/◎ | ○/◎ | ○/◎ | △/△ | ×/× |
| Pearlescent pigment | ◎/◎ | ◎/◎ | ◎/◎ | △/△ | ×/× |
| Amihope?LL | ◎/◎ | ◎/◎ | ◎/◎ | △/△ | ×/× |
| Red No. 202 | ○/◎ | ○/◎ | ○/◎ | △/△ | ×/× |
Table 1-5: water repellency and hydrophilic result of the test
| Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) | |
| Sericite FSE | 5 | 5 | 5 | 5 | 5 |
| Muscovitum Y-2300 | 4 | 4 | 4 | 5 | 5 |
| Talcum JA-46R | 5 | 5 | 5 | 5 | 5 |
| Titanium CR-50 | 5 | 5 | 5 | 5 | 5 |
| Yellow LL-100P | 5 | 5 | 5 | 5 | 5 |
| Red R-516PS | 5 | 5 | 5 | 5 | 5 |
| Black BL-100P | 5 | 5 | 5 | 5 | 5 |
| The micropartical titanium oxide | 5 | 5 | 5 | 5 | 5 |
| The micropartical titanium oxide | 1 | 1 | 1 | 5 | 5 |
| The micropartical titanium oxide | 1 | 1 | 1 | 5 | 5 |
| The micropartical zinc oxide | 5 | 5 | 5 | 5 | 5 |
| Pearlescent pigment | 5 | 5 | 5 | 5 | 5 |
| Amihope?LL | 1 | 1 | 1 | 5 | 5 |
| Red No. 202 | 4 | 4 | 4 | 5 | 5 |
The surface-treated powder that embodiment 1-9 and 1-10 and embodiment 1-13 are obtained has hydrophilic oil repellent.The surface-treated powder that each embodiment obtained all has higher usability and adaptation.
[embodiment 1-15～1-32 and comparative example 1-15～1-32]
Secondly, the embodiment to the cosmetics that are mixed with surface-treated powder of the present invention describes.Based on each composition of following table, make various cosmetics by following method for making.
In addition, about the cosmetics that each embodiment and comparative example obtained, finish effect, cosmetic persistence at usability, cosmetic, for 20 professional sensory test persons are respectively prepared in each evaluation, please it make and apply some make up 1 day, and estimate according to the metewand shown in following table 1-6～table 1-8, whole sensory test persons' summation score is obtained divided by 20 to mark.
Table 1-6: the evaluation of usability
| Benchmark | Scoring |
| Usability is very good | ◎ |
| Usability is good | ○ |
| Usability is common | ● |
| Usability is poor | △ |
| The non-constant of usability | × |
Table 1-7: make up and finish Evaluation on effect
| Benchmark | Scoring |
| Sensation produces effect very much | ◎ |
| Feel to produce effect | ○ |
| Sensation produces effect slightly | ● |
| Only feel small effect | △ |
| Sensation to no effect | × |
About finishing the project of effect, at making up and the skin care cosmetics are to estimate the uniformity of finishing effect, protection, the reflecting feel of nature, the uniformity of cosmetic film, at the hidroschesis cosmetics is to estimate to have or not the adhesion sense, have or not greasy feeling, is to estimate reflecting feel, dry feeling, smoothness, easy comb property at cosmetic hair.
Table 1-8: the evaluation of cosmetic persistence
| Benchmark | Scoring |
| Sensation produces effect very much | ◎ |
| Feel to produce effect | ○ |
| Sensation produces effect slightly | ● |
| Only feel small effect | △ |
| Sensation to no effect | × |
The project of cosmetic muffin is made as and prevents colour of skin dimness, prevents that secondary from adhering to (gamut), preventing glossy these 3 projects.In addition, be to estimate to be difficult for fissility at the manicure product.
The manufacturing of (embodiment 1-15 and comparative example 1-15) muffin
Make the muffin of forming shown in the table 1-9 by following method.Evaluation result is shown in table 1-10.
Table 1-9
| Composition | Weight portion |
| (1) sericite (embodiment 1-1 and comparative example 1-1) | 35.0 |
| (2) Talcum (embodiment 1-3 and comparative example 1-3) | Surplus |
| (3) titanium oxide (embodiment 1-4 and comparative example 1-4) | 8.5 |
| (4) yellow iron oxide (embodiment 1-5 and comparative example 1-5) | 3.5 |
| (5) red iron oxide (embodiment 1-6 and comparative example 1-6) | 1.8 |
| (6) black iron oxide (embodiment 1-7 and comparative example 1-7) | 0.2 |
| (7) myristic acid octyl group dodecyl ester | 4.0 |
| (8) squalane | 3.5 |
| (9) methyl phenyl silicone | 1.5 |
| (10) antiseptic | In right amount |
| (11) spice | In right amount |
(method for making)
Pulverize with mentioned component (1)～(6) mixing and by pulverizer.It is transferred in the high speed blender, adds the further mix homogeneously of material that composition (7)～(11) heating mix homogeneously is got.It is fed pulverizer, sieve and after making the granularity unanimity, the surface pressing with 10MPa in aluminium ware carries out compression molding, make dual-purpose muffin.
Table 1-10
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ○ | ◎ | △ | △ |
| Finish the uniformity of effect | ○ | ○ | ◎ | ● | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
The manufacturing of (embodiment 1-16 and comparative example 1-16) oil-in-water type foundation cream
Make the w/o type foundation emulsion of forming shown in the table 1-11 by following method.Evaluation result is shown in table 1-12.
Table 1-11
| Composition | Weight portion |
| (1) decamethylcyclopentaandoxane | 20.0 |
| (2) vaseline | 0.5 |
| (3) methyl phenyl silicone | 2.3 |
| (4) squalane | 4.2 |
| (5) different n-nonanoic acid isotridecyl ester | 4.5 |
| (6) dimethyl polysiloxane polyoxyalkylene polymers (HLB=4.5) | 3.0 |
| (7) red iron oxide (embodiment 1-6 and comparative example 1-6) | 1.3 |
| (8) yellow iron oxide (embodiment 1-5 and comparative example 1-5) | 2.4 |
| (9) black iron oxide (embodiment 1-7 and comparative example 1-7) | 0.1 |
| (10) titanium oxide (embodiment 1-4 and comparative example 1-4) | 8.0 |
| (11) Talcum (embodiment 1-3 and comparative example 1-3) | 2.5 |
| (12) ethanol | 5.0 |
| (13) 1,3 butylene glycol | 5.0 |
| (14) sodium chloride | 2.0 |
| (15) purified water | Surplus |
| (16) Amihope LL (embodiment 1-13 and comparative example 1-13) | 5.0 |
| (17) antiseptic | In right amount |
| (18) spice | In right amount |
(method for making)
Mentioned component (7)～(11) are pre-mixed pulverizing.Mixture to composition (1)～(6) being dissolved equably composition (7)～(11) that adding crushes in advance in the oil phase that mixes under 70 ℃ utilizes the homodisperse machine that it is disperseed equably.Will be under 70 ℃ with composition (12)～(17) equably the water that forms of mixed dissolution slowly be added in the above-mentioned oil phase, utilize the homogenizer homodisperse after, cool off, add composition (18) and granulate and become emulsified particle, make foundation emulsion.
Table 1-12
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ◎ | ○ | ◎ | △ | △ |
| Finish the uniformity of effect | ○ | ◎ | ◎ | × | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | △ | △ |
| Quality stability * 1 | Well | Well | Well | Difference | Difference |
* 1 quality stability is to place for 1 week afterwards to observe viscosity and separation, sedimentation in 50 ℃ temperature chamber.Being designated as of no cosmetic variation is good.The cosmetics that are mixed with the chemical compound (d) of comparative example and processing powder body (e) separated next day, and quality stability is poor.
The manufacturing of (embodiment 1-17 and comparative example 1-17) eye shadow
Make the eye shadow of forming shown in the table 1-13 by following method.Evaluation result is shown in table 1-14.
Table 1-13
| Composition | Weight portion |
| 1. decamethylcyclopentaandoxane | 15.0 |
| 2. dimethyl polysiloxane (6cs) | 10.0 |
| 3. polyether-modified poly-silica * 2 | 2.0 |
| 4.PEG (10) Laurel ether | 0.5 |
| 5. titanium oxide (embodiment 1-4 and comparative example 1-4) | 2.5 |
| 6. red iron oxide (embodiment 1-6 and comparative example 1-6) | 3.5 |
| 7. pearlescent pigment (embodiment 1-12 and comparative example 1-12) | 6.0 |
| 8. sodium chloride | 2.0 |
| 9. propylene glycol | 8.0 |
| 10. antiseptic | In right amount |
| 11. spice | In right amount |
| 12. purified water | Surplus |
* 2 KF6026: SHIN-ETSU HANTOTAI's chemical industry system
(method for making)
(1) composition 1～4 is mixed, adding ingredient 5～7 also disperses equably.
(2) composition 8～10 and composition 12 are dissolved equably.
(3) mixture that under agitation (2) is obtained slowly is added in the mixture that (1) obtained, and carries out emulsifying and adding ingredient 11 and obtains eye shadow.
Table 1-14
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ◎ | ○ | ○ | △ | × |
| Finish the uniformity of effect | ○ | ◎ | ◎ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ● | ○ |
The manufacturing of the solid shape foundation cream of (embodiment 1-18 and comparative example 1-18) oiliness
Make the solid shape foundation cream of the oiliness of forming shown in the table 1-15 by following method.Evaluation result is shown in table 1-16.
Table 1-15
| Composition | Weight portion |
| (1) isopropyl palmitate | 20.0 |
| (2) spermol | 7.0 |
| (3) squalane | 15.5 |
| (4) polyglycereol three isostearates | 5.0 |
| (5) the different paraffin of volatile liquid | 10.0 |
| (6) ceresine | 3.8 |
| (7) candelilla wax | 5.5 |
| (8) red iron oxide (embodiment 1-6 and comparative example 1-6) | 0.8 |
| (9) titanium oxide (embodiment 1-4 and comparative example 1-4) | 11.5 |
| (10) Talcum (embodiment 1-3 and comparative example 1-3) | 8.0 |
| (11) antiseptic | In right amount |
| (12) spice | In right amount |
(method for making)
Mentioned component (8)～(10) are pre-mixed pulverizing.To under 85 ℃, adding composition (8)～(11) crush in advance and utilize the homodisperse machine to disperse equably in the oil phase that composition (1)～(7) mixed dissolution forms.To wherein adding spice, recharge to metalware, make the solid shape foundation cream of oiliness and cool off.
Table 1-16
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ◎ | ○ | ○ | △ | × |
| Finish the uniformity of effect | ○ | ◎ | ◎ | ● | × |
| The cosmetic persistence | ◎ | ◎ | ◎ | ● | ○ |
The manufacturing of (embodiment 1-19 and comparative example 1-19) oil-in-water type sunscreen cream (sunscreen cream)
Make the oil-in-water type sunscreen cream of forming shown in the table 1-17 by following method.Evaluation result is shown in table 1-18.
Table 1-17
| Composition | Weight portion |
| 1. the different paraffin of volatile liquid (Fancol ID) | 15.0 |
| 2. polydimethylsiloxane (6cs) | 2.0 |
| 3. isononyl isononanoate | 3.5 |
| 4. spermol | 1.0 |
| 5. squalane | 5.0 |
| 6. polyethylene glycol mono stearate (4EO) | 1.0 |
| 7. poly-Semen Ricini linoleic acid six polyglycerin ester | 3.5 |
| 8. micropartical titanium oxide HFE dispersion * 3 | 10.0 |
| 9. micropartical zinc oxide (embodiment 1-11 and comparative example 1-11) | 15.0 |
| 10. purified water | Surplus |
| 11. glycerol | 5.0 |
| 12.1, the 3-butanediol | 5.0 |
| 13. ketopyrrolidine sodium formate | 2.5 |
| 14. antiseptic | In right amount |
| 15. spice | In right amount |
* 3 with the micropartical titanium oxide of embodiment 1-8 and comparative example 1-8 and hydrogen fluorine ether (HFE7200: Sumitomo 3M company) disperse in sand mill with the composition of 30: 70 (weight portion) and make dispersion.Pigment-dispersing ability and storage stability height by the surface-treated powder that specific fluorinated copolymer of the present invention was covered.
To dissolve down at 75 ℃ except that the oil-phase component of composition (1)～(9) the composition (8).The water-phase component of composition (10)～(14) is dissolved down at 75 ℃, be added into after the homogenization in the oil-phase component, carry out emulsifying with homogenizer.Add composition (8) and (15) at last and cool off and make sunscreen cream.
Table 1-18
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ◎ | ○ | ○ | △ | × |
| Finish the uniformity of effect | ○ | ◎ | ◎ | ● | × |
| The cosmetic persistence | ◎ | ◎ | ◎ | ● | ○ |
| The spf value * 4 of preparation | 23 | 25 | 26 | 20 | 15 |
* 4 so-called external spf values are meant the numerical value of the screening effect that shows ultraviolet (UVB), and this value is high more, and then ultraviolet screening effect is good more.The operation of 3M company is attached on the quartz glass plate with adhesive tape (surgical tape), at 0.08g/cm
2Condition under sunscreen cream is coated on the adhesive tape face, measure with the SPF analyser of U.S. Optometrics company.
The manufacturing of (embodiment 1-20 and comparative example 1-20) eye-liner
Make the eye-liner of forming shown in the table 1-19 by following method.Evaluation result is shown in table 1-20.
Table 1-19
| Composition | Weight portion |
| (1) decamethylcyclopentaandoxane | 25.0 |
| (2) dimethyl polysiloxane (6cs) | 4.0 |
| (3) Simmondsia chinensis oil | 2.5 |
| (4) polyether-modified poly-silica * 5 | 1.0 |
| (5) black iron oxide (embodiment 1-7 and comparative example 1-7) | 20.0 |
| (6) ethanol | 5.0 |
| (7) antiseptic | In right amount |
| (8) purified water | Surplus |
* 5 KF6026: SHIN-ETSU HANTOTAI's chemical industry system
(method for making)
(1) composition 1～4 is mixed down at 70 ℃, add composition 5 and dispersion equably.
(2) composition 6～8 is heated mixed dissolution down at 70 ℃.
(3) mixture that under agitation (2) is obtained slowly is added in the mixture that (1) obtained, and carries out emulsifying and obtains eye-liner.
Table 1-20
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ○ | ○ | △ | × |
| Finish the uniformity of effect | ○ | ◎ | ◎ | △ | × |
| The cosmetic persistence | ◎ | ◎ | ◎ | △ | ○ |
The manufacturing of (embodiment 1-21 and comparative example 1-21) lipstick
Make the lipstick of forming shown in the table 1-21 by following method.Evaluation result is shown in table 1-22.
Table 1-21
(method for making)
(1) composition 7～9 is added in the composition 1, mixes and it is disperseed equably with roller.
(2) with behind other composition heating mixed dissolution, add mentioned component (1) and utilize homogenizer to disperse equably.
(3) after the degassing, pour in the mould and obtain lip stick.
Table 1-22
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ○ | ○ | ● | ● |
| Finish the uniformity of effect | ○ | ◎ | ◎ | △ | × |
| The cosmetic persistence | ◎ | ◎ | ◎ | △ | ○ |
The manufacturing of (embodiment 1-22 and comparative example 1-22) lip coat
Make the lip coat of forming shown in the table 1-23 by following method.Evaluation result is shown in table 1-24.
Table 1-23
| Composition | Weight portion |
| (1) PFPE (Fomblin HC-04) | 91.5 |
| (2) silicon dioxide (Aerosil R-972) * 6 | 2.0 |
| (3) micropartical titanium oxide (embodiment 1-8 and comparative example 1-8) | 6.0 |
| (4) glycerol | 1.0 |
* 6 methods of mixing by embodiment 1-1 and comparative example 1-1 have been carried out the surface-treated material to be respectively each fluorochemical (a1)～(e1) of 5%.
(method for making)
In composition (1) adding ingredient (2) and composition (3) and disperse equably after, add composition (4) and make lip coat.
Table 1-24
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ○ | ○ | ○ | ● |
| Finish the uniformity of effect | ○ | ◎ | ◎ | △ | × |
| The cosmetic persistence | ◎ | ◎ | ◎ | △ | ○ |
The manufacturing of (embodiment 1-23 and comparative example 1-23) oil-in-water type foundation emulsion
Make the O/W type foundation emulsion of forming shown in the table 1-25 by following method.Evaluation result is shown in table 1-26.
Table 1-25
| Composition | Weight portion |
| (1) stearic acid | 1.5 |
| (2) spermol | 1.0 |
| (3) Tween-81 (3EO) | 1.0 |
| (4) Span-83 | 1.0 |
| (5) liquid paraffin | 5.0 |
| (6) 2 ethyl hexanoic acid glyceride | 5.0 |
| (7) glycerol | 5.0 |
| (8) 1,3 butylene glycol | 5.0 |
| (9) acrylic acid-alkyl methacrylate (C 10～30) copolymer | 0.05 |
| (10) locust bean gum | 0.2 |
| (11) triethanolamine | 0.8 |
| (12) antiseptic | In right amount |
| (13) purified water | Surplus |
| (14) titanium oxide (embodiment 1-4 and comparative example 1-4) | 5.0 |
| (15) yellow iron oxide (embodiment 1-5 and comparative example 1-5) | 1.0 |
| (16) red iron oxide (embodiment 1-6 and comparative example 1-6) | 0.3 |
| (17) black iron oxide (embodiment 1-7 and comparative example 1-7) | 0.1 |
| (18) Amihope LL (embodiment 1-13 and comparative example 1-13) | 5.0 |
(method for making)
A: with composition (1)～(6) heating for dissolving.
B: with composition (7)～(13) heating for dissolving equably.
C: add the mixture that B obtained in the mixture that A obtained, the cooling back adds composition (14)～(18), mixes equably and makes foundation emulsion.
Table 1-26
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ○ | ○ | ○ | ● |
| Finish the uniformity of effect | ○ | ◎ | ◎ | △ | × |
| The cosmetic persistence | ◎ | ◎ | ◎ | △ | ○ |
The manufacturing of (embodiment 1-24 and comparative example 1-24) colour of skin emulsion
Make the colour of skin emulsion of forming shown in the table 1-27 by following method.Evaluation result is shown in table 1-28.
Table 1-27
| Composition | Weight portion |
| (1) N-stearyl-L-glutamic acid | 0.5 |
| (2) spermol | 0.5 |
| (3) polyoxyethylene (10 moles) monostearate | 0.8 |
| (4) ten polyglycereol list isostearates | 1.0 |
| (5) Span-83 | 0.4 |
| (6) methyl phenyl silicone | 5.0 |
| (7) glycerol | 5.0 |
| (8) 1,3 butylene glycol | 5.0 |
| (9) Xanthan gum | 0.1 |
| (10) carrageenin | 0.05 |
| (11) triethanolamine | 1.0 |
| (12) antiseptic | In right amount |
| (13) purified water | Surplus |
| (14) titanium oxide (embodiment 1-4 and comparative example 1-4) | 2.0 |
| (15) yellow iron oxide (embodiment 1-5 and comparative example 1-5) | 1.0 |
| (16) red iron oxide (embodiment 1-6 and comparative example 1-6) | 0.5 |
| (17) black iron oxide (embodiment 1-7 and comparative example 1-7) | 0.1 |
| (18) Talcum (embodiment 1-3 and comparative example 1-3) | 3.0 |
(method for making)
A: with composition (1)～(6) heating for dissolving.
B: with composition (7)～(13) heating for dissolving equably.
C: add the mixture that B obtained in the mixture that A obtained, the cooling back adds composition (14)～(18), mixes equably and makes colour of skin emulsion.
Table 1-28
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ◎ | ○ | ○ | △ | △ |
| Finish the uniformity of effect | ○ | ◎ | ◎ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
The manufacturing of (embodiment 1-25 and comparative example 1-25) manicure product
Make the manicure product of forming shown in the table 1-29 by following method.Evaluation result is shown in table 1-30.
Table 1-29
| Composition | Weight portion |
| (1) NC Nitroncellulose | 10.0 |
| (2) alkyd resins | 10.0 |
| (3) acetyl tributyl citrate | 4.0 |
| (4) dl-Camphora | 1.0 |
| (5) organically-modified Strese Hofmann's hectorite. | 1.0 |
| (6) ethyl acetate | 20.0 |
| (7) butyl acetate | Surplus |
| (8) isopropyl alcohol | 5.0 |
| (9) red No. 202 (embodiment 1-14 and comparative example 1-14) | 0.1 |
| (10) titanium oxide (embodiment 1-4 and comparative example 1-4) | 3.0 |
| (11) pearlescent pigment (embodiment 1-12 and comparative example 1-12) | 5.0 |
| (12) red iron oxide (embodiment 1-6 and comparative example 1-6) | 0.5 |
(method for making)
Utilizing dispersion machine that composition (1)～(9) are mixed stirs.To wherein adding composition (10)～(12), utilize dispersion machine to mix 10 minutes and manufacturing manicure product, and be filled in the vial.
Table 1-30
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ○ | ○ | △ | △ |
| Finish the uniformity of effect | ○ | ○ | ○ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
In addition, the manicure product that are mixed with the surface-treated powder that is covered by specific fluorinated copolymer of the present invention can be in time through and form hard cake, dispersion stabilization is good.
The manufacturing of (embodiment 1-26 and comparative example 1-26) rouge
Make the rouge of forming shown in the table 1-31 by following method.Evaluation result is shown in table 1-32.
Table 1-31
| Composition | Weight portion |
| (1) Muscovitum (embodiment 1-2 and comparative example 1-2) | 14.0 |
| (2) titanium oxide (embodiment 1-4 and comparative example 1-4) | 10.0 |
| (3) yellow iron oxide (embodiment 1-5 and comparative example 1-5) | 1.0 |
| (4) red iron oxide (embodiment 1-6 and comparative example 1-6) | 0.5 |
| (5) black iron oxide (embodiment 1-7 and comparative example 1-7) | 0.1 |
| (6) Talcum (embodiment 1-3 and comparative example 1-3) | Surplus |
| (7) PFPE (Fomblin HC-04) | 7.0 |
| (8) dimethyl polysiloxane (10 CS) | 5.0 |
(method for making)
Composition (1)～(6) uniform mixing is pulverized.After wherein adding composition (7), (8) and uniform mixing, pulverize and make rouge.
Table 1-32
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ○ | ○ | × | × |
| Finish the uniformity of effect | ◎ | ◎ | ○ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
The manufacturing of (embodiment 1-27 and comparative example 1-27) hidroschesis cosmetics
Make the bar-shaped hidroschesis cosmetics of forming shown in the table 1-33 by following method.Evaluation result is shown in table 1-34.
Table 1-33
| Composition | Weight portion |
| (1) Brazil wax | 1.0 |
| (2) ceresine | 6.0 |
| (3) paraffin | 3.0 |
| (4) sorbitan sesquialter isostearate | 2.5 |
| (5) 2 ethyl hexanoic acid cetyl | 27.0 |
| (6) squalane | 2.0 |
| (7) decamethylcyclopentaandoxane | Surplus |
| (8) polymeric aluminum chloride | 25.0 |
| (9) sericite (embodiment 1-1 and comparative example 1-1) | 10.0 |
| (10) Talcum (embodiment 1-3 and comparative example 1-3) | 8.0 |
| (11) micropartical zinc oxide (embodiment 1-11 and comparative example 1-11) | 2.0 |
| (12) antioxidant | In right amount |
| (13) spice | In right amount |
(method for making)
Composition (1)～(7) are heated and uniform dissolution.After wherein adding composition (8)～(12) and uniform mixing, add composition (13) and cool off and make bar-shaped hidroschesis cosmetics.
Table 1-34
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ◎ | ○ | × | × |
| Finish the uniformity of effect | ◎ | ◎ | ○ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
The manufacturing of (embodiment 1-28 and comparative example 1-28) hair care breast (hair treatment)
Make the hair care breast of forming shown in the table 1-35 by following method.Evaluation result is shown in table 1-36.
Table 1-35
| Composition | Weight portion |
| (1) glycol distearate | 1.0 |
| (2) liquid paraffin | 10.0 |
| (3) squalane | 5.0 |
| (4) stearyl alcohol | 1.5 |
| (5) dimethyl polysiloxane (10cs) | 3.0 |
| (6) stearic acid | 6.0 |
| (7) polyoxyethylene (3) stearyl alcohol | 4.5 |
| (8) polyoxyethylene (150) cetyl ether | 2.0 |
| (9) organic modified bentonite | 0.2 |
| (10) Amihope LL (embodiment 1-13 and comparative example 1-13) | 2.0 |
| (11) 1,3 butylene glycol | 6.0 |
| (12) antiseptic | In right amount |
| (13) spice | In right amount |
| (14) purified water | Surplus |
(method for making)
A: composition (1)～(9) are heated and uniform dissolution.To wherein adding composition (10) and homodisperse.
B: composition (11), (12), (14) heating are mixed.
C: after in the mixture that A obtained, add mixing the mixture that B obtained and cooling off, add composition (13) and cool off and make the hair care breast.
Table 1-36
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ◎ | ○ | × | × |
| Finish the uniformity of effect | ◎ | ◎ | ◎ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | △ | ● |
The manufacturing of (embodiment 1-29 and comparative example 1-29) colour of skin beautifying liquid
Make the colour of skin that table forms shown in the 1-37 beautifying liquid of preserving moisture by following method.Evaluation result is shown in table 1-38.
Table 1-37
| Composition | Weight portion |
| (1) purified water | Surplus |
| (2) acrylic acid/alkyl methacrylate (C 10～30) copolymer | 0.1 |
| (3) CVP Carbopol ETD2050 | 1.0 |
| (4) antiseptic | In right amount |
| (5) particulate titanium dioxide (embodiment 1-9 and comparative example 1-9) | 1.0 |
| (6) triethanolamine | 0.7 |
| (7) glycerol | 25.0 |
| (8) titanium oxide (1-4 and comparative example 1-4) | 2.0 |
| (9) yellow iron oxide (embodiment 1-5 and comparative example 1-5) | 0.8 |
| (10) red iron oxide (embodiment 1-6 and comparative example 1-6) | 0.3 |
| (11) black iron oxide (embodiment 1-7 and comparative example 1-7) | 0.1 |
| (12) Talcum (embodiment 1-3 and comparative example 1-3) | 3.5 |
(method for making)
A: composition (1)～(4) heating after the uniform dissolution, is added composition (5) and homodisperse and mixes.Adding composition (6) neutralizes.
B: behind composition (8)～(12) uniform mixing, add composition (7) and uniform mixing.
C: in the mixture that A obtained, add to mix the mixture that B obtained, make the colour of skin beautifying liquid of preserving moisture.
Table 1-38
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ○ | ○ | × | × |
| Finish the uniformity of effect | ◎ | ◎ | ◎ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ● | ○ |
The manufacturing of (embodiment 1-30 and comparative example 1-30) aqueous eye shadow
Make the aqueous eye shadow of forming shown in the table 1-39 of aqueous by following method.Evaluation result is shown in table 1-40.
Table 1-39
| Composition | Weight portion |
| (1) purified water | Surplus |
| (2) acrylic acid/alkyl methacrylate (C 10～30) copolymer | 0.1 |
| (3) CVP Carbopol ETD2050 | 1.0 |
| (4) antiseptic | In right amount |
| (5) triethanolamine | 0.7 |
| (6) glycerol | 25.0 |
| (7) titanium oxide (embodiment 1-4 and comparative example 1-4) | 2.5 |
| (8) red iron oxide (embodiment 1-6 and comparative example 1-6) | 2.0 |
| (9) pearlescent pigment (embodiment 1-12 and comparative example 1-12) | 8.0 |
(method for making)
A: composition (1)～(4) heating after the uniform dissolution, is added composition (5) and uniform mixing.
B: behind composition (7)～(9) uniform mixing, add composition (6) and uniform mixing.
C: in the mixture that A obtained, add and mix the mixture that B obtained, make aqueous aqueous eye shadow.
Table 1-40
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ○ | ○ | △ | △ |
| Finish the uniformity of effect | ◎ | ◎ | ◎ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
The manufacturing of (embodiment 1-31 and the comparative example 1-31) powder of whitening
Make the powder of forming shown in the table 1-41 of whitening by following method.Evaluation result is shown in table 1-42.
Table 1-41
| Composition | Weight portion |
| (1) L-magnesium L-ascorbyl-2-phosphate (magnesium L-ascorbyl phosphate) | 1.0 |
| (2) sodium citrate | 1.0 |
| (3) 1,3 butylene glycol | 5.0 |
| (4) glycerol | 5.0 |
| (5) purified water | Surplus |
| (6) methyl parahydroxybenzoate | 0.2 |
| (7) Muscovitum (embodiment 1-2 and comparative example 1-2) | 5.0 |
| (8) Talcum (embodiment 1-3 and comparative example 1-3) | 0.1 |
| (9) organopolysiloxane elastomer powder | 3.0 |
| (10) three fluoro-alkyl dimethyl trimethyl silicane alcoxyl base esters of silicon acis | 3.0 |
| (11) partially crosslinked organopolysiloxane polymer * 7 | 5.0 |
| (12) red iron oxide (embodiment 1-6 and comparative example 1-6) | 0.5 |
* 7 KSG-16 (chemical industrial company of SHIN-ETSU HANTOTAI system)
(method for making)
A: composition (7)～(9) are mixed, pulverized.
B: behind composition (11)～(12) uniform mixing, be added in the mixture that above-mentioned A obtains.
C: composition (1)～(6) are mixed, dissolved.
D: the mixture that above-mentioned B obtained is mixed with the mixture that C is obtained, be filled in the container and obtain to whiten powder.
Table 1-42
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ○ | ○ | ○ | △ | △ |
| Finish the uniformity of effect | ◎ | ◎ | ◎ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
The manufacturing of (embodiment 1-32 and comparative example 1-32) anti-Exposure to Sunlight frost
Make the anti-Exposure to Sunlight frost of forming shown in the table 1-43 by following method.Evaluation result is shown in table 1-44.
Table 1-43
* 8 utilize sand mill to disperse the compositions of micropartical titanium oxide/purified water/glycerol=45/50/5 of embodiment 1-10 and comparative example 1-10 and make aqueous dispersion.The aqueous dispersion of embodiment can be not in time through and settlement separate, comparatively stable.The dispersion of the dispersion of comparative example does not go on, and fails to form even and stable dispersion.
(method for making)
A: with composition (3)～(7) heating, mixing.
B: behind composition (1) and (2), (6) uniform mixing, be added in the mixture that above-mentioned A obtains.
C: composition (8)～(12) are mixed, dissolved.
D: in the mixture that above-mentioned B obtained, add the mixture that C obtained and carry out emulsifying, obtain anti-Exposure to Sunlight frost.
Table 1-44
| Assessment item | Chemical compound (a1) | Chemical compound (b1) | Chemical compound (c1) | Chemical compound (d1) | Chemical compound (e1) |
| Usability | ◎ | ◎ | ◎ | × | × |
| Finish the uniformity of effect | ◎ | ◎ | ◎ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | △ | △ |
| Quality stability * 9 | ◎ | ◎ | ◎ | × | × |
* 9 quality stability be in 50 ℃ temperature chamber, place 1 week the back observe the having that it's too late and separate of crystallization, the sedimentation of UV absorbent.The cosmetics of cosmetic variation such as no crystallization are designated as well.Crystallization took place and produces separation next day in the cosmetics that are mixed with the chemical compound (d1) of comparative example and processing powder body (e1), and quality stability is poor.
(embodiment 1-33 and comparative example 1-33)
The Talcum JA-13R of 100g (shallow field powder process company) is fed in the 500g water of being prepared in the glass beaker of 2L, stirs fully and make its dispersion.Slowly add count the lysate of IPA of the fluorinated copolymer of the Production Example 1-4 of 3g and comparative example chemical compound (e1) and 10g with solid constituent after, stirred 15 minutes.Glass beaker is transferred on the hot plate,, treats to keep this temperature after temperature reaches 80 ℃ with the condition intensification of 3 ℃/min.(in the temperature-rise period, the chemical compound (a1) to (d1) that has oxygen base ethylidene in the molecular structure of the polymer of surface conditioning agent dewaters because of the cloud point phenomenon, wrap powder particle and be covered processing) stirring was kept 15 minutes after, dewater, clean, dry (115 ℃/16 hours), utilize super micron mill to pulverize, obtain each fluorochemical and handle Talcum.
(embodiment 1-34 and comparative example 1-34)
The Talcum JA-13R of 100g (shallow field powder process company) is fed in the 500g water of being prepared in the glass beaker of 2L, stirs fully and make its dispersion.Slowly add count the lysate of IPA of the fluorinated copolymer of the Production Example 1-4 of 3g and comparative example chemical compound (e1) and 10g with solid constituent after, stirred 15 minutes.Then, one side is kept stirring, and the NaCl that one side is slowly added 30g is dissolved in the solution that forms in the water of 100g.(in the slowly interpolation process, the chemical compound (a1) to (d1) that has oxygen base ethylidene in the molecular structure of the polymer of surface conditioning agent dewaters because of salting-out phenomenon, wrap powder particle and be covered processing) stirring was kept 15 minutes after, dewater, clean, dry (115 ℃/16 hours), utilize super micron mill to pulverize, obtain each fluorochemical and handle Talcum.
(embodiment 1-35 and comparative example 1-35)
The Talcum JA-13R of 100g (shallow field powder process company) is fed in the 500g water of being prepared in the glass beaker of 2L, stirs fully and make its dispersion.Slowly add count the lysate of IPA of the fluorinated copolymer of the Production Example 1-4 of 3g and comparative example chemical compound (e2) and 10g with solid constituent after, stirred 15 minutes.Thus obtained slurry is supplied to the spray dryer that possesses the two-fluid spray nozzle.The inlet hot blast temperature of spray dryer is made as 200 ℃, and the atomisation pressure of two-fluid spray nozzle is made as 0.6MPa.Obtain each fluorochemical thus and handle Talcum.
(embodiment 1-36 and comparative example 1-36)
Utilize kneader that the water of the Talcum JA-13R of 5kg (shallow field powder process company) and 5kg is mixed and make slurry.Input is counted the Production Example 1-4 of 3g and the fluorinated copolymer of comparative example chemical compound (e1) with solid constituent, utilizes stone mortar type grater Supermasscolloider (MKCA 6-2: increase good fortune industry company) to carry out mechanochemistry (mechanochemical) and handles.The slurry that is obtained is utilized vacuum vibrating dryer drying.Obtain each fluorochemical thus and handle Talcum.
(embodiment 1-37 and comparative example 1-37)
Drop into titanyl sulfate (titanyl sulfate) crystallization in the water and heat, the hydrolysate that is generated is filtered, cleans, in the oxidizing aqueous titanium filter cake that is obtained (titanium oxide content is 100g) of 350g, one side stirs 48% sodium hydrate aqueous solution that one side adds 400g, and heating was also stirred 2 hours in 95～105 ℃ scope.Then, filter, clean the suspension of this titanium dioxide hydrates.Add the water of 500g and make slurry to filter cake, and then simultaneously stir 35% hydrochloric acid that one side drops into 140g, under 95 ℃, added thermal maturation 2 hours through cleaning.The aqueous suspension concentration of the micropartical titanium oxide that obtained is adjusted into 70g/L.In this aqueous suspension, add polyaluminium chloride (with respect to the micropartical titanium oxide, with Al
2O
3Count 10 weight %), and then use caustic soda pH to be adjusted to 5.0, ripening 30 minutes.After the ripening, drop into respect to the micropartical titanium oxide and count the Production Example 1-4 of amount of 7 weight % and the fluorinated copolymer of comparative example chemical compound (e1), ripening 30 minutes with solid constituent.Filter, clean, drying, utilize the ECK super micron mill to pulverize.Obtain each fluorochemical thus and handle the micropartical titanium oxide.
The manufacturing of (embodiment 1-38 and comparative example 1-38) anti-Exposure to Sunlight condensation
Make the anti-Exposure to Sunlight condensation of forming shown in the table 1-45 by following method.Evaluation result is shown in table 1-46.
Table 1-45
(method for making)
Composition (1)～(4) are heated to 80 ℃ and dissolving.Composition (5) and (6) are heated to 80 ℃ and dissolving.The composition (5) that adds in mentioned component (1)～(4) through heating for dissolving neutralizes with (6).Composition (7) to (9) is heated to 80 ℃ and mixing dispersion., carry out emulsifying and obtain anti-Exposure to Sunlight condensation to (9) to above-mentioned these compositions (7) that in neutral composition, slowly add with homogenizer.
Table 1-46
| Assessment item | Embodiment | Comparative example |
| Usability | ◎ | △ |
| Finish the uniformity of effect | ○ | △ |
| The cosmetic persistence | ◎ | △ |
| The external spf value of preparation | 20 | 15 |
| Stable * 10 in time | ○ | × |
* 10 this preparation preserved 1 month down at 50 ℃.The character of outward appearance is unconverted to be designated as zero, vicissitudinous being designated as *.
The manufacturing of (embodiment 1-39 and comparative example 1-39) wet forming muffin
Make the foundation cream of forming shown in the table 1-47 by following method.Evaluation result is shown in table 1-48.
Table 1-47
(method for making)
A: composition (7) and (8) are heated to 75 ℃, and dissolving equably.
B: utilize mixer that micronizing is carried out in composition (1)～(6) mixing.
C: one side utilizes mixer that above-mentioned B is stirred, and one side is added A and homodisperse.
D: with respect to the composition of the C of 100 weight portions, the purified water of adding 100 weight portions, uniform mixing and make pulp-like.
E: above-mentioned D is filled in the metalware, places absorbent paper and pressurization on the surface and remove a part of purified water.
F: above-mentioned F was placed 24 hours in 30 ℃ temperature chamber, remove purified water fully, obtain the wet forming muffin.
Table 1-48
| Assessment item | Embodiment | Comparative example |
| Usability | ◎ | △ |
| Finish the uniformity of effect | ○ | △ |
| The cosmetic persistence | ◎ | △ |
The manufacturing of (embodiment 1-40 and comparative example 1-40) F/W emulsifying emulsion
Make the emulsion of forming shown in the table 1-49 by following method.Evaluation result is shown in table 1-50.
Table 1-49
| Composition | Weight portion |
| (1) PFPE (Fomblin HC/04: Su Wei company) | 25.0 |
| (2) hydrogen fluorine ether (CF-76:3M company) | 10.0 |
| (3) Talcum JA-13R (embodiment 1-34 and comparative example 1-34) | 6.0 |
| (4) ethanol | 10.0 |
| (5) glycerol | 3.5 |
| (6) purified water | To 100.0 |
| (7) antiseptic | In right amount |
(method for making)
A: with composition (1)～(3) uniform mixing and be heated to 50 ℃.
B: composition (4)～(7) are utilized the mixing of homogenizer dispersing and dissolving and are heated to 50 ℃.
C: one side utilizes homogenizer that above-mentioned B is stirred, and one side is slowly added above-mentioned A, obtains F/W emulsifying emulsion.
Table 1-50
| Assessment item | Embodiment | Comparative example |
| Usability | ◎ | △ |
| Finish the uniformity of effect | ○ | △ |
| The cosmetic persistence | ◎ | × |
The manufacturing of (embodiment 1-41 and comparative example 1-41) W/F emulsifying emulsion
Make the emulsion of forming shown in the table 1-51 by following method.Evaluation result is shown in table 1-52.
Table 1-51
| Composition | Weight portion |
| (1) PFPE (Fomblin HC/04: Su Wei company) | 45.0 |
| (2) hydrogen fluorine ether (CF-76:3M company) | 15.0 |
| (3) Talcum (embodiment 1-35 and comparative example 1-35) | 5.5 |
| (4) ethanol | 5.0 |
| (5) glycerol | 3.5 |
| (6) purified water | To 100.0 |
| (7) antiseptic | In right amount |
(method for making)
A: with composition (1)～(3) uniform mixing and be heated to 50 ℃.
B: composition (4)～(7) are utilized the mixing of homogenizer dispersing and dissolving and are heated to 50 ℃.
C: one side utilizes homogenizer that above-mentioned A is stirred, and one side is slowly added above-mentioned B, obtains W/F emulsifying emulsion.
Table 1-52
| Assessment item | Embodiment | Comparative example |
| Usability | ◎ | △ |
| Finish the uniformity of effect | ○ | △ |
| The cosmetic persistence | ◎ | × |
The manufacturing of (embodiment 1-42 and comparative example 1-42) powder body emulsifying sunscreen cream
Make the emulsion of forming shown in the table 1-53 by following method.Evaluation result is shown in table 1-54.
Table 1-53
(method for making)
A: composition (1)～(5) are utilized the dispersion machine uniform mixing and are heated to 50 ℃.
B: composition (6)～(9) are heated to 50 ℃ and uniform mixing.
C: one side utilizes homogenizer that above-mentioned A is stirred, and one side is slowly added above-mentioned B, obtains powder body emulsifying sunscreen cream.
Table 1-54
| Assessment item | Embodiment | Comparative example |
| Usability | ◎ | △ |
| Finish the uniformity of effect | ○ | △ |
| The cosmetic persistence | ◎ | △ |
[Production Example 2-1～2-3]
List the Production Example of employed fluorinated copolymer chemical compound among the present invention as follows.
[Production Example 2-1]
Take into account the fluorochemical monomer CH of the 18.6g that packs in the 100ml four-hole boiling flask of agitating device to possessing reflux cooling pipe, nitrogen ingress pipe, temperature
2=CHC (=O) O-CH
2CH
2C
6F
13The polyethylene glycol acrylate CH of (below be designated as C6SFA (a)), 11.4g
2=CHC (=O) O-(CH
2CH
2O)
n-H (meansigma methods of n is 2, below is designated as AE90 (b) for Blemmer AE90, day oily limited company manufacturing), the lauryl mercaptan of 0.3g and the isopropyl alcohol of 45g carry out nitrogen foaming in 30 minutes.After under nitrogen current, interior temperature being warming up to 50～65 ℃, add the Perbutyl PV (below be designated as PV) of 0.4g, 60～65 ℃ of reactions 10 hours down.The solution that is obtained is removed isopropyl alcohol in about 70 ℃ of following distillations under reduced pressure, after obtaining faint yellow polymer residue, add the water of 122.4g, after 80 ℃ of following maintenances of interior Wen Zaiyue are more than 1 hour, cool off, make the aqueous dispersions that solid component concentration is about 20 weight %.
[Production Example 2-2]
Take into account AE90 (b), the polyethylene glycol acrylate CH of 5.7g of C6SFA (a), the 5.7g of the 18.6g that packs in the 100ml four-hole boiling flask of agitating device to possessing reflux cooling pipe, nitrogen ingress pipe, temperature
2=CHC (=O) O-(CH
2CH
2O)
n-H (Blemmer AE200, day oily limited company makes, and the meansigma methods of n is 4.5, below is designated as AE200 (b)), the lauryl mercaptan of 0.3g and the isopropyl alcohol of 45g, carry out the polyreaction same, make the aqueous dispersions that solid component concentration is about 20 weight % with Production Example 2-1.
[Production Example 2-3]
Take into account AE350 (b), the polyethyleneglycol diacrylate CH of 0.9g of C6SFA (a), the 10.5g of the 18.6g that packs in the 100ml four-hole boiling flask of agitating device to possessing reflux cooling pipe, nitrogen ingress pipe, temperature
2=CHC (=O) O-(CH
2CH
2O)
n-C (=O) CH=CH
2(meansigma methods of n is 7 for Blemmer ADE300, day oily limited company manufacturing), the lauryl mercaptan of 0.3g and the isopropyl alcohol of 45g carry out the polyreaction same with Production Example 2-1, make the aqueous dispersions that solid component concentration is about 20 weight %.
Table 2-1
[embodiment 2-1～2-14 and comparative example 2-1～2-14]
(a2)～(c2) of table shown in the 2-1 is each fluorinated copolymer used in the present invention, (d2) and the copolymer (e2) be the chemical compound of existing (comparative example).Manufacturing is carried out the surface-treated powder body through above-mentioned each chemical compound, estimates each rerum natura of these surface-treated powders.List the manufacturing embodiment of surface-treated powder and assessment item and method as follows.In addition, will utilize the surface treatment that employed fluorinated copolymer carried out among the present invention shown in the above-mentioned table 2-1 to be designated as the FAW processing among the embodiment.
The evaluation methodology of handling powder body is as follows.
(the contact angle test of water and squalane)
, to metalware, exerted pressure for 10 seconds and form powder filled, and on this profiled surface, drip water or squalane, measure drop and powder surface angulation with the pressure of 6MPa.The contact angle meter (CA-D) that utilizes consonance interface science company to make drips water or squalane (dripping quantity is 10 μ l) at this shaping powder surface, measures drop and powder body coated face angulation after 20 seconds.(the n number is made as 5) drop is absorbed by powder body and the situation that can't measure contact angle is designated as infiltration.
(usability and fitness test)
By 15 sensory test persons that can carry out the sensory test of surface-treated powder, estimate the usability and the adaptation of each surface-treated powder at same powder body.Evaluation methodology is by to refer to that abdomen rubs, and perhaps coats fingernail or upper arm parts and carries out.Evaluation is that the absolute evaluation by each sensory test person carries out, and its scoring is as follows.◎: very good, zero: good, △: common, *: poor.
(water repellency and hydrophilic evaluation methodology)
The purified water that in the glass beaker of 100cc, adds about 50cc.On the water surface, drop into the processing powder body of about 0.1g, utilize spatula with each second about 2 times frequency stir.Estimate the muddy degree that stirs the water after 50 times, 100 times, 150 times with 5 grades.
＜metewand 〉
5 waters are not seen muddiness.(water repellency is strong)
4 waters are seen muddiness slightly.
3 waters are visible significantly muddy.
2 most of powder body are transferred to aqueous phase.
1 whole powder body are transferred to aqueous phase.(hydrophilic is strong)
(evaluation result)
In the embodiment that the results are shown in of the contact angle of water and squalane test respectively handled powder body and the hurdle of comparative example.The result of the test of usability and adaptation is that the evaluation guide look is shown in table 2-18.
(embodiment 2-1 (FAW handles sericite) and comparative example 2-1)
Counting 1g (adding ratio (Japanese: outside cut) 1 weight %) with solid constituent to the mode that increases progressively 1g between the 5g (adding ratio 5 weight %) at every turn with the surface treatment amount that will show each fluorinated copolymer shown in the 2-1, the sericite FSE (three letter miner companies) of 100g is being handled.In each fluorinated copolymer, add the water of 50g and mixed 30 minutes.To mix thing at 80 ℃ down after dry 3 hours, so 110 ℃ dry 10 hours down.Carry out micronizing then, obtain each fluorinated copolymer and handle sericite.Show the result in table 2-2 and table 2-3.
The result of table 2-2:(embodiment 2-1 and comparative example 2-1)
Each fluorinated copolymer is handled the contact angle test of sericite and water/squalane
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 16 °/infiltration | 50°/35° | 140°/130° | 72°/140° | Permeate/145 ° |
| Chemical compound of the present invention (b2) | 18 °/infiltration | 48°/37° | 137°/133° | 64°/139° | Permeate/142 ° |
| Chemical compound of the present invention (c2) | 15 °/infiltration | 55°/38° | 136°/122° | 75°/139° | Permeate/140 ° |
| The chemical compound of comparative example (d2) | 17 °/infiltration | 53°/42° | 137°/123° | 138°/135° | 145°/133° |
| The chemical compound of comparative example (e2) | 20 °/infiltration | 83°/56° | 141°/128° | 143°/140° | 140°/142° |
As show shown in the 2-2, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 2% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 3% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 5% o'clock.Even if treating capacity is increased to more than 5%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-3.
Table 2-3: the result of embodiment 2-1 and comparative example 2-1
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of sericite
| 1％ | 2％ | 3％ | 4％ | 5％ |
| Chemical compound of the present invention (a2) | 1 | 3 | 4 | 2 | 1 |
| Chemical compound of the present invention (b2) | 1 | 3 | 4 | 2 | 1 |
| Chemical compound of the present invention (c2) | 1 | 3 | 4 | 2 | 1 |
| The chemical compound of comparative example (d2) | 1 | 3 | 4 | 5 | 5 |
| The chemical compound of comparative example (e2) | 1 | 3 | 4 | 5 | 5 |
(embodiment 2-2 (FAW handles titanium) and comparative example 2-2)
Counting 1g (adding ratio 1 weight %) with solid constituent to the mode that increases progressively 1g between the 5g (adding ratio 5 weight %) at every turn with the surface treatment amount that will show each fluorinated copolymer shown in the 2-1, the titanium CR-50 (the former industry of stone company) of 100g is being handled.Each fluorochemical is added with the water dilution back of 10ml.Utilize mixer to mix after 15 minutes, import 250 ℃ superheated vapour, the moment that reaches 200 ℃ in mixer stops to stir, and obtains each fluorinated copolymer and handles titanium.Show the result in table 2-4 and table 2-5.
Table 2-4: the result of embodiment 2-2 and comparative example 2-2
Each fluorinated copolymer is handled the contact angle test of titanium and water/squalane
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 16 °/infiltration | 61°/35° | 140°/133° | 72°/141° | Permeate/142 ° |
| Chemical compound of the present invention (b2) | 18 °/infiltration | 64°/37° | 143°/136° | 64°/140° | Permeate/143 ° |
| Chemical compound of the present invention (c2) | 15 °/infiltration | 78°/38° | 141°/131° | 75°/137° | Permeate/142 ° |
| The chemical compound of comparative example (d2) | 20 °/infiltration | 89°/56° | 138°/135° | 147°/140° | 148°/142° |
| The chemical compound of comparative example (e2) | 24 °/infiltration | 80°/42° | 137°/140° | 148°/142° | 143°/143° |
As show shown in the 2-4, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 2% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 3% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 5% o'clock.Even if treating capacity is increased to more than 5%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-5.
Table 2-5: the result of embodiment 2-2 and comparative example 2-2
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of titanium
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 1 | 2 | 4 | 2 | 1 |
| Chemical compound of the present invention (b2) | 1 | 3 | 5 | 3 | 1 |
| Chemical compound of the present invention (c2) | 1 | 2 | 4 | 2 | 1 |
| The chemical compound of comparative example (d2) | 1 | 3 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 1 | 3 | 5 | 5 | 5 |
(embodiment 2-3 (FAW handles yellow iron oxide) and comparative example 2-3)
Counting 2g (adding ratio 2 weight %) with solid constituent to the mode that increases progressively 1g between the 6g (adding ratio 6 weight %) at every turn, to yellow iron oxide (the yellow LL-100P: handle of 100g titanium industrial group) with the surface treatment amount that will show each fluorinated copolymer shown in the 2-1.Each fluorochemical is added with the water dilution back of 5ml.Utilize Henschel mixer to mix after 15 minutes, drying is 10 hours under 110 ℃, utilizes super micron mill to pulverize then, obtains each fluorinated copolymer and handles yellow iron oxide.Show the result in table 2-6 and table 2-7.
Table 2-6: the result of embodiment 2-3 and comparative example 2-3
Each fluorinated copolymer is handled the contact angle test of yellow iron oxide and water/squalane
| 2％ | 3％ | 4％ | 5％ | 6％ | |
| Chemical compound of the present invention (a2) | 16 °/infiltration | 61°/35° | 132°/116° | 61°/141° | Permeate/142 ° |
| Chemical compound of the present invention (b2) | 18 °/infiltration | 64°/37° | 131°/124° | 55°/140° | Permeate/143 ° |
| Chemical compound of the present invention (c2) | 17 °/infiltration | 85°/42° | 130°/126° | 68°/138° | Permeate/143 ° |
| The chemical compound of comparative example (d2) | 20 °/infiltration | 89°/56° | 139°/135° | 148°/140° | 144°/142° |
| The chemical compound of comparative example (e2) | 24 °/infiltration | 80°/42° | 138°/128° | 147°/142° | 145°/143° |
As show shown in the 2-6, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 3% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 4% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 6% o'clock.Even if treating capacity is increased to more than 6%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-7.
Table 2-7: the result of embodiment 2-3 and comparative example 2-3
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of yellow iron oxide
| 2％ | 3％ | 4％ | 5％ | 6％ | |
| Chemical compound of the present invention (a2) | 1 | 2 | 4 | 2 | 1 |
| Chemical compound of the present invention (b2) | 1 | 2 | 5 | 3 | 1 |
| Chemical compound of the present invention (c2) | 1 | 2 | 4 | 2 | 1 |
| The chemical compound of comparative example (d2) | 1 | 3 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 1 | 3 | 5 | 5 | 5 |
(embodiment 2-4 (FAW handles red iron oxide) and comparative example 2-4)
Counting 2g (adding ratio 2 weight %) with solid constituent to the mode that increases progressively 1g between the 6g (adding ratio 6 weight %) at every turn with the surface treatment amount that will show each fluorinated copolymer shown in the 2-1, the red iron oxide of 100g (red R-516PS: Japanese titanium industrial group) is being handled.Below by handling with the same method of embodiment 2-3, obtain each fluorinated copolymer and handle red iron oxide.Show the result in table 2-8 and table 2-9.
Table 2-8: the result of embodiment 2-4 and comparative example 2-4
Each fluorinated copolymer is handled the contact angle test of red iron oxide and water/squalane
| 2％ | 3％ | 4％ | 5％ | 6％ | |
| Chemical compound of the present invention (a2) | 18 °/infiltration | 66°/35° | 140°/133° | 72°/141° | Permeate/142 ° |
| Chemical compound of the present invention (b2) | 14 °/infiltration | 75°/38° | 141°/131° | 75°/137° | Permeate/142 ° |
| Chemical compound of the present invention (c2) | 25 °/infiltration | 76°/42° | 141°/130° | 74°/138° | Permeate/143 ° |
| The chemical compound of comparative example (d2) | 26 °/infiltration | 80°/56° | 138°/135° | 143°/140° | 145°/142° |
| The chemical compound of comparative example (e2) | 28 °/infiltration | 82°/42° | 137°/140° | 138°/142° | 143°/143° |
As show shown in the 2-8, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 3% water repellency when following and oil repellent are low by powder body that fluoropolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 4% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 6% o'clock.Even if treating capacity is increased to more than 6%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-9.
The result of table 2-9:(embodiment 2-4 and comparative example 2-4)
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of red iron oxide
| 2％ | 3％ | 4％ | 5％ | 6％ | |
| Chemical compound of the present invention (a2) | 1 | 3 | 4 | 2 | 1 |
| Chemical compound of the present invention (b2) | 1 | 3 | 4 | 3 | 1 |
| Chemical compound of the present invention (c2) | 1 | 2 | 4 | 2 | 1 |
| The chemical compound of comparative example (d2) | 1 | 3 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 1 | 3 | 5 | 5 | 5 |
(embodiment 2-5 (FAW handles black iron oxide) and comparative example 2-5)
Counting 1g (adding ratio 1 weight %) with solid constituent to the mode that increases progressively 1g between the 5g (adding ratio 5 weight %) at every turn with the surface treatment amount that will show each fluorinated copolymer shown in the 2-1, the black iron oxide of 100g (black BL-100P: Japanese titanium industrial group) is being handled.Below by handling with the same method of embodiment 2-3, obtain each fluorinated copolymer and handle black iron oxide.Show the result in table 2-10 and table 2-11.
Table 2-10: the result of embodiment 2-5 and comparative example 2-5
Each fluorinated copolymer is handled the contact angle test of black iron oxide and water/squalane
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 35 °/infiltration | 134°/128° | 68°/133° | 12°/141° | Permeate/142 ° |
| Chemical compound of the present invention (b2) | 40 °/infiltration | 136°/125° | 70°/136° | 13°/140° | Permeate/143 ° |
| Chemical compound of the present invention (c2) | 45 °/infiltration | 138°/130° | 64°/138° | 15°/137° | Permeate/142 ° |
| The chemical compound of comparative example (d2) | 68 °/infiltration | 140°/134° | 146°/145° | 145°/140° | 145°/142° |
| The chemical compound of comparative example (e2) | 57 °/infiltration | 142°/133° | 144°/140° | 146°/142° | 143°/143° |
As show shown in the 2-10, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 1% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 2% o'clock in treating capacity.Be 4% and showed hydrophilic oil repellent at 5% o'clock in treating capacity.Even if treating capacity is increased to more than 5%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-11.
Table 2-11: the result of embodiment 2-5 and comparative example 2-5
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of black iron oxide
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 1 | 3 | 5 | 2 | 1 |
| Chemical compound of the present invention (b2) | 2 | 3 | 5 | 2 | 1 |
| Chemical compound of the present invention (c2) | 1 | 3 | 5 | 2 | 1 |
| The chemical compound of comparative example (d2) | 2 | 3 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 2 | 3 | 5 | 5 | 5 |
(embodiment 2-6 (FAW handles the micropartical titanium oxide) and comparative example 2-6)
Micropartical titanium oxide (MT-500SA: chemical company of kingdom) be fed in the deionized water (sodium hexameta phosphate that contains 0.05g) of 1500ml, again each fluorinated copolymer of counting 6g with solid constituent added with the IPA dilution back of 500ml with 100g.Utilize sand mill (DYNO-Mill:1.4L zirconium oxide Rong Qi ﹠amp; Blade, the zirconium oxide bead of 0.5mm φ, filling rate are 85%) disperse by 15 minutes circulations.This dispersion liquid under agitation is heated to 80 ℃, drips the 10%HCl aqueous solution and pH is adjusted to 4.5.After dewatering by centrifugalize, 120 ℃ dry 16 hours and utilize the JET super micron mill to pulverize down, obtain each fluorinated copolymer and handle micropartical titanium oxide.In addition, also manufactured experimently and handling the surface-treated powder that forms each fluorinated copolymer amount is increased progressively 1% mode between 6% to 10% at every turn under the above-mentioned treatment conditions.Show the result in table 2-12 and table 2-13.
Table 2-12: the result of embodiment 2-6 and comparative example 2-6
Each fluorinated copolymer is handled the contact angle test of micropartical titanium oxide and water/squalane
| 6％ | 7％ | 8％ | 9％ | 10％ | |
| Chemical compound of the present invention (a2) | 35 °/infiltration | 134°/128° | 88°/133° | 29°/141° | Permeate/142 ° |
| Chemical compound of the present invention (b2) | 40 °/infiltration | 136°/125° | 80°/136° | 25°/143° | Permeate/143 ° |
| Chemical compound of the present invention (c2) | 45 °/infiltration | 138°/130° | 94°/138° | 25°/139° | Permeate/142 ° |
| The chemical compound of comparative example (d2) | 68 °/infiltration | 140°/134° | 146°/145° | 145°/140° | 145°/142° |
| The chemical compound of comparative example (e2) | 57 °/infiltration | 142°/133° | 144°/140° | 146°/142° | 143°/143° |
As show shown in the 2-12, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 6% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 7% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 10% o'clock.Even if treating capacity is increased to more than 10%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-13.
Table 2-13: the result of embodiment 2-6 and comparative example 2-6
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of micropartical titanium oxide
| 6％ | 7％ | 8％ | 9％ | 10％ | |
| Chemical compound of the present invention (a2) | 2 | 5 | 4 | 2 | 1 |
| Chemical compound of the present invention (b2) | 2 | 5 | 4 | 2 | 1 |
| Chemical compound of the present invention (c2) | 2 | 5 | 4 | 2 | 1 |
| The chemical compound of comparative example (d2) | 3 | 5 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 3 | 5 | 5 | 5 | 5 |
(embodiment 2-7 (FAW processing/SA handles the micropartical zinc oxide) and comparative example 2-7)
Chemical company of kingdom), the degree of polymerization in that single end has a triethoxy that is respectively each fluorinated copolymer shown in the table 2-1 of 5g to 9g, 3g with solid component meter is to add the water of 20g and the IPA of 50g in 15 the straight chain shape dimethyl polysiloxane (SA processing), utilizes kneader to mix 30 minutes to the micropartical zinc oxide of 100g (MZ-300:.After the deionized water that adds 10g again mixed 30 minutes, carry out the JET micronizing after dry 16 hours down, obtain the Combined Processing micropartical zinc oxide of each fluorinated copolymer and silicone at 105 ℃.Show the result in table 2-14 and table 2-15.
Table 2-14: the result of embodiment 2-7 and comparative example 2-7
Each fluorinated copolymer is handled the contact angle test of micropartical zinc oxide and water/squalane
| 5％ | 6％ | 7％ | 8％ | 9％ | |
| Chemical compound of the present invention (a2) | 75°/25° | 144°/135° | 98°/133° | 51°/141° | Permeate/142 ° |
| Chemical compound of the present invention (b2) | 85°/26° | 148°/136° | 102°/138° | 62°/137° | Permeate/142 ° |
| Chemical compound of the present invention (c2) | 77°/27° | 145°/137° | 87°/137° | 54°/138° | Permeate/143 ° |
| The chemical compound of comparative example (d2) | 88°/30° | 140°/140° | 146°/145° | 145°/140° | 145°/142° |
| The chemical compound of comparative example (e2) | 97°/38° | 142°/142° | 144°/140° | 146°/142° | 143°/143° |
As show shown in the 2-14, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 5% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 6% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 9% o'clock.Even if treating capacity is increased to more than 9%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-15.
Table 2-15: the result of embodiment 2-7 and comparative example 2-7
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of micropartical zinc oxide
| 5％ | 6％ | 7％ | 8％ | 9％ | |
| Chemical compound of the present invention (a2) | 3 | 5 | 3 | 2 | 1 |
| Chemical compound of the present invention (b2) | 3 | 5 | 3 | 2 | 1 |
| Chemical compound of the present invention (c2) | 3 | 5 | 3 | 2 | 1 |
| The chemical compound of comparative example (d2) | 4 | 5 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 4 | 5 | 5 | 5 | 5 |
(embodiment 2-8 (FAW processing/NAI handles Margarita) and comparative example 2-8)
With the pearlescent pigment of 100g (Flamencogold: Engelhardt company) be added in the deionized water of 1000ml, add again 1.0g N-stearyl disodium glutamate (aginomoto company: Amisoft HS-21P) (NAI processing) dissolve dispersion.Add each fluorinated copolymer shown in 1g to the 5g table 2-1 again and heat, utilize kneader to mix 30 minutes to 80 ℃.Then, the Al that adds 0.5mol/L
2(SO
4) 3 aqueous solutions and the pH of the thing that will mix is adjusted to 5.0.Drying is 8 hours under 140 ℃, obtains the Combined Processing pearlescent pigment of each fluorinated copolymer and acylated amino acid.Show the result in table 2-16 and table 2-17.
Table 2-16: the result of embodiment 2-8 and comparative example 2-8
Each fluorinated copolymer is handled the contact angle test of little Margarita and water/squalane
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 50°/15° | 144°/136° | 98°/133° | 51°/137° | Permeate/142 ° |
| Chemical compound of the present invention (b2) | 46°/10° | 146°/132° | 90°/136° | 45°/141° | Permeate/143 ° |
| Chemical compound of the present invention (c2) | 40°/16° | 148°/133° | 102°/138° | 52°/140° | Permeate/142 ° |
| The chemical compound of comparative example (d2) | 88°/30° | 148°/145° | 149°/146° | 145°143° | 145°/142° |
| The chemical compound of comparative example (e2) | 97°/38° | 148°/142° | 146°/141° | 146°/142° | 143°/143° |
As show shown in the 2-16, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 1% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 2% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 5% o'clock.Even if treating capacity is increased to more than 5%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-17.
Table 2-17: the result of embodiment 2-8 and comparative example 2-8
Each fluorinated copolymer is handled water repellency and the hydrophilic result of the test of little Margarita
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 2 | 5 | 3 | 2 | 1 |
| Chemical compound of the present invention (b2) | 2 | 5 | 3 | 2 | 1 |
| Chemical compound of the present invention (c2) | 2 | 5 | 3 | 2 | 1 |
| The chemical compound of comparative example (d2) | 3 | 5 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 3 | 5 | 5 | 5 | 5 |
(embodiment 2-9 (FAW handles lauroyl lysine) and comparative example 2-9)
To the Amihope of 100g LL (lauroyl lysine: add aginomoto company) that IPA/ utilizes NaOH and the mixed liquor that is adjusted to aqueous solution=15g/10g of pH ≒ 8.0, and each fluorinated copolymer shown in adding 1g to the 5g table 2-1, method by embodiment 2-8 and comparative example 2-8 is similarly carried out surface treatment, obtains each fluorochemical and handles Amihope LL.Show the result in table 2-18 and table 2-19.
Table 2-18: the result of embodiment 2-9 and comparative example 2-9:
Each fluorinated copolymer is handled the contact angle test of lauroyl lysine and water/squalane
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 75°/25° | 144°/135° | 98°/133° | 51°/141° | Permeate/142 ° |
| Chemical compound of the present invention (b2) | 85°/36° | 148°/136° | 102°/138° | 62°/137° | Permeate/142 ° |
| Chemical compound of the present invention (c2) | 77°/27° | 145°/137° | 87°/137° | 54°/138° | Permeate/143 ° |
| The chemical compound of comparative example (d2) | 88°/30° | 140°/140° | 146°/145° | 145°/140° | 145°/142° |
| The chemical compound of comparative example (e2) | 97°/38° | 142°/142° | 144°/140° | 146°/142° | 143°/143° |
As show shown in the 2-18, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 1% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 2% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 5% o'clock.Even if treating capacity is increased to more than 5%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-19.
Table 2-19: the result of embodiment 2-9 and comparative example 2-9
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of lauroyl lysine
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 4 | 5 | 3 | 2 | 1 |
| Chemical compound of the present invention (b2) | 4 | 5 | 3 | 2 | 1 |
| Chemical compound of the present invention (c2) | 4 | 5 | 3 | 2 | 1 |
| The chemical compound of comparative example (d2) | 4 | 5 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 4 | 5 | 5 | 5 | 5 |
(embodiment 2-10 (FAW handles red No. 202) and comparative example 2-10)
The redness No. 202 (changing into company the sixth of the twelve Earthly Branches in the last of the ten Heavenly stems) of 100g is added in the mixed solution of IPA/ deionized water=40g/100g, and one side utilizes propeller-type mixer to stir, and one side utilizes Soniprep (Japanese Waja company) to disperse.Each fluorinated copolymer shown in Dropwise 5 g to the 9g table 2-1 and the IPA of 5g, carry out ripening after, by heating in vacuum distill remove desolvate and 105 ℃ dry down, pulverized 16 hours, obtain each fluorinated copolymer and handle redness No. 202.Show the result in table 2-20 and table 2-21.
Table 2-20: the result of embodiment 2-10 and comparative example 2-10
Each fluorinated copolymer is handled red No. 202 and is tested with the contact angle of water/squalane
| 5％ | 6％ | 7％ | 8％ | 9％ | |
| Chemical compound of the present invention (a2) | 75°/25° | 144°/135° | 98°/133° | 51°/141° | Permeate/142 ° |
| Chemical compound of the present invention (b2) | 85°/36° | 148°/136° | 102°/138° | 62°/137° | Permeate/142 ° |
| Chemical compound of the present invention (c2) | 77°/27° | 145°/137° | 87°/137° | 54°/138° | Permeate/143 ° |
| The chemical compound of comparative example (d2) | 88°/30° | 140°/140° | 146°/145° | 145°/140° | 145°/142° |
| The chemical compound of comparative example (e2) | 97°/38° | 142°/142° | 144°/140° | 146°/142° | 143°/143° |
As show shown in the 2-20, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 5% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 6% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 9% o'clock.Even if treating capacity is increased to more than 9%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-21.
Table 2-21: the result of embodiment 2-10 and comparative example 2-10
Each fluorinated copolymer is handled red No. 202 water repellency and hydrophilic result of the test
| 5％ | 6％ | 7％ | 8％ | 9％ | |
| Chemical compound of the present invention (a2) | 3 | 5 | 4 | 3 | 1 |
| Chemical compound of the present invention (b2) | 3 | 5 | 4 | 3 | 1 |
| Chemical compound of the present invention (c2) | 3 | 5 | 4 | 3 | 1 |
| The chemical compound of comparative example (d2) | 4 | 5 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 4 | 5 | 5 | 5 | 5 |
(embodiment 2-11 (FAW processing/ALS handles the mixture of polymethyl siloxane/vinyldimethicone and titanium oxide) and comparative example 2-11)
With the Dimethicone/Vinyl Dimethicone of 100g and the mixture (Dow Corning Corporation of titanium oxide; EP-9261 TI Cosmetic Powder) in the high-speed mixer of packing into, adding will with solid constituent count each fluorinated copolymer shown in the table 2-1 of 1g to 5g and with the triethoxy caprylyl silane of 1g (Dow Corning Corporation: Z-6341) (ALS processing) be dissolved in the solution that forms among the IPA (isopropyl alcohol) of 10g and stirred 5 minutes.One side is kept stirring, and one reduces pressure in the face of in the groove, is warming up to 50 ℃ and stirred 15 minutes.The powder body that is obtained is carried out micronizing, obtain the Combined Processing Dimethicone/Vinyl Dimethicone of each fluoropolymer treated and alkyl silane and the mixture powder of titanium oxide.Show the result in table 2-22 and table 2-23.
Table 2-22: the result of embodiment 2-11 and comparative example 2-11
Each fluorinated copolymer handle polymethyl siloxane/vinyldimethicone with
The mixture of titanium oxide and the test of the contact angle of water/squalane
| 1％ | 2％ | 3％ | ?4％ | 5％ | |
| Chemical compound of the present invention (a2) | 45 °/infiltration | 94°/65° | 145°/133° | ?51°/141° | Permeate/140 ° |
| Chemical compound of the present invention (b2) | 41 °/infiltration | 98°/66° | 148°/138° | ?62°/137° | Permeate/141 ° |
| Chemical compound of the present invention (c2) | 42 °/infiltration | 85°/57° | 145°/137° | ?54°/138° | Permeate/138 ° |
| The chemical compound of comparative example (d2) | 58 °/infiltration | 90°/70° | 146°/145° | ?144°/140° | 142°/142° |
| The chemical compound of comparative example (e2) | 67 °/infiltration | 102°/82° | 144°/140° | ?146°/142° | 143°/143° |
As show shown in the 2-22, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 2% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 3% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 5% o'clock.Even if treating capacity is increased to more than 5%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-23.
The result of table 2-23 embodiment 2-11 and comparative example 2-11
The mixture of each fluorinated copolymer processing polymethyl siloxane/vinyldimethicone and titanium oxide
Water repellency and hydrophilic result of the test
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 2 | 3 | 4 | 2 | 1 |
| Chemical compound of the present invention (b2) | 2 | 3 | 5 | 2 | 1 |
| Chemical compound of the present invention (c2) | 2 | 3 | 5 | 2 | 1 |
| The chemical compound of comparative example (d2) | 2 | 3 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 2 | 3 | 5 | 5 | 5 |
(embodiment 2-12 (FAW processing/C6F silane treatment micropartical zinc oxide) and comparative example 2-12)
In the micropartical zinc oxide MZ-300 of 100g (chemical company of kingdom), add with solid constituent and count each fluorinated copolymer shown in the table 2-1 of 3g to 6g, ten trifluoro octyltri-ethoxysilane (the Dynasylan F-8261: the water of (C6F silane treatment) and 60g/IPA=1/1 solution Evonik Degussa Corp.) of 5g, utilize kneader to mix 60 minutes, drying is 16 hours under 130 ℃.Carry out micronizing then, obtain the Combined Processing micropartical zinc oxide of each fluorinated copolymer and C6F silane.Show the result in table 2-24 and table 2-25.
Table 2-24: the result of embodiment 2-12 and comparative example 2-12
Each fluorinated copolymer is handled the contact angle test of micropartical zinc oxide and water/squalane
| 3％ | 4％ | 5％ | 6％ | 7％ | |
| Chemical compound of the present invention (a2) | 149°/144° | 108°/145° | 89°/145° | 41°/150° | Permeate/141 ° |
| Chemical compound of the present invention (b2) | 150°/146° | 102°/143° | 78°/147° | 32°/148° | Permeate/143 ° |
| Chemical compound of the present invention (c2) | 158°/147° | 110°/142° | 80°/140° | 34°/140° | Permeate/140 ° |
| The chemical compound of comparative example (d2) | 154°/149° | 154°/146° | 146°/145° | 144°/140° | 142°/142° |
| The chemical compound of comparative example (e2) | 156°/146° | 157°/145° | 144°/145° | 146°/142° | 143°/143° |
As show shown in the 2-24, even if the processing powder body that utilizes the fluorinated copolymer of comparative example to handle increases treating capacity, water and oil repellant is no change also, is 3% water repellency when following and oil repellent height by powder body that fluorinated copolymer of the present invention was covered in the treating capacity of fluorinated copolymer.C6F silane treatment amount be 5% and the treating capacity of fluorinated copolymer be to show the highest water and oil repellant at 3% o'clock.In the treating capacity of fluorinated copolymer is to show hydrophilic oil repellent at 7% o'clock.Even if treating capacity is increased to more than 7%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-25.
Table 2-25: the result of embodiment 2-12 and comparative example 2-12
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of micropartical zinc oxide
| 3％ | 4％ | 5％ | 6％ | 7％ | |
| Chemical compound of the present invention (a2) | 5 | 4 | 3 | 2 | 1 |
| Chemical compound of the present invention (b2) | 5 | 4 | 3 | 2 | 1 |
| Chemical compound of the present invention (c2) | 5 | 4 | 3 | 2 | 1 |
| The chemical compound of comparative example (d2) | 5 | 5 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 5 | 5 | 5 | 5 | 5 |
(embodiment 2-13 (FAW handles sericite) and comparative example 2-13)
By powder body and the method shown in the embodiment 2-1, except utilizing NaOH the pH of mixed solution (50: the 50 weight %) 50g of IPA and water is adjusted to 8.5, similarly handle, obtain fluorinated copolymer and handle sericite.Show the result in table 2-26 and table 2-27.
Table 2-26: the result of embodiment 2-13 and comparative example 2-13
Each fluorinated copolymer is handled the contact angle test of sericite and water/squalane
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 26 °/infiltration | 30°/45° | Permeate/140 ° | Permeate/140 ° | Permeate/145 ° |
| Chemical compound of the present invention (b2) | 28 °/infiltration | 38°/42° | Permeate/141 ° | Permeate/139 ° | Permeate/142 ° |
| Chemical compound of the present invention (c2) | 25 °/infiltration | 35°/40° | Permeate/140 ° | Permeate/139 ° | Permeate/140 ° |
| The chemical compound of comparative example (d2) | 28 °/infiltration | 53°/52° | 101°/143° | 138°/145° | 145°/143° |
| The chemical compound of comparative example (e2) | 25 °/infiltration | 43°/59° | 105°/145° | 143°/142° | 140°/142° |
As show shown in the 2-26, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 2% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is 3% to show high hydrophilic oil repellent when above in treating capacity.Even if treating capacity is increased to more than 5%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-27.
Table 2-27: the result of embodiment 2-13 and comparative example 2-13
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of sericite
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 2 | 2 | 1 | 1 | 1 |
| Chemical compound of the present invention (b2) | 2 | 2 | 1 | 1 | 1 |
| Chemical compound of the present invention (c2) | 2 | 2 | 1 | 1 | 1 |
| The chemical compound of comparative example (d2) | 2 | 3 | 4 | 5 | 5 |
| The chemical compound of comparative example (e2) | 2 | 3 | 4 | 5 | 5 |
(embodiment 2-14 (FAW handles Talcum) and comparative example 2-14)
The Talcum JA-13R of 100g (shallow field powder process company) is fed in the 500g water of being prepared in the glass beaker of 2L, stirs fully and make its dispersion.Slowly add count the lysate of IPA of each fluorinated copolymer shown in the table 2-1 of 1g to 5g and 10g with solid constituent after, stirred 15 minutes.Thus obtained slurry is supplied to the spray dryer that possesses the two-fluid spray nozzle.The inlet hot blast temperature of spray dryer is made as 200 ℃, and the atomisation pressure of two-fluid spray nozzle is made as 0.6MPa.Obtain each fluorinated copolymer thus and handle Talcum.Show the result in table 2-28 and table 2-29.
Table 2-28: the result of embodiment 2-14 and comparative example 2-14
Each fluorinated copolymer is handled the contact angle test of Talcum and water/squalane
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 29 °/infiltration | 48°/65° | 55°/95° | 61°/100° | Permeate/101 ° |
| Chemical compound of the present invention (b2) | 30 °/infiltration | 42°/63° | 67°/87° | 72°/108° | Permeate/103 ° |
| Chemical compound of the present invention (c2) | 38 °/infiltration | 40°/62° | 58°/86° | 64°/100° | Permeate/103 ° |
| The chemical compound of comparative example (d2) | 44 °/infiltration | 94°/76° | 143°/97° | 144°/110° | 142°/112° |
| The chemical compound of comparative example (e2) | 56 °/infiltration | 97°/75° | 144°/95° | 146°/112° | 143°/113° |
As show shown in the 2-28, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 2% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 3% o'clock in treating capacity.Be that treating capacity is to show hydrophilic oil repellent at 5% o'clock.Even if treating capacity is increased to more than 5%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-29.
2-29: the result of embodiment 2-14 and comparative example 2-14
Each fluorinated copolymer is handled steatitic water repellency and hydrophilic result of the test
| 1％ | 2％ | 3％ | 4％ | 5％ | |
| Chemical compound of the present invention (a2) | 2 | 2 | 3 | 3 | 1 |
| Chemical compound of the present invention (b2) | 2 | 2 | 3 | 3 | 1 |
| Chemical compound of the present invention (c2) | 2 | 2 | 3 | 3 | 1 |
| The chemical compound of comparative example (d2) | 2 | 3 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 2 | 3 | 5 | 5 | 5 |
(embodiment 2-15 (FAW handles the micropartical titanium oxide) and comparative example 2-15)
Drop into the titanyl sulfate crystallization in the water and heat, the hydrolysate that is generated is filtered, cleans, in the oxidizing aqueous titanium filter cake that is obtained (titanium oxide content is 100g) of 350g, one side stirs 48% sodium hydrate aqueous solution that one side adds 400g, heating was stirred 2 hours in 95～105 ℃ scope.Then, filter, clean the suspension of this titanium dioxide hydrates.Add the water of 500g and make slurry to filter cake, and then simultaneously stir 35% hydrochloric acid that one side drops into 140g, under 95 ℃, added thermal maturation 2 hours through cleaning.The aqueous suspension concentration of the micropartical titanium oxide that obtained is adjusted into 70g/L.In this aqueous suspension, add polyaluminium chloride (with respect to the micropartical titanium oxide, with Al
2O
3Count 10 weight %), and then use caustic soda pH to be adjusted to 5.0, ripening 30 minutes.After the ripening, drop into respect to the micropartical titanium oxide and count each fluorinated copolymer shown in the table 2-1 of amount of 6～10 weight %, ripening 30 minutes with solid constituent.Filter, clean, drying, utilize the ECK super micron mill to pulverize.Obtain each fluorinated copolymer thus and handle the micropartical titanium oxide.Show the result in table 2-30 and table 2-31.
Table 2-30: the result of embodiment 2-15 and comparative example 2-15
Each fluorinated copolymer is handled the contact angle test of micropartical titanium oxide and water/squalane
| 6％ | 7％ | 8％ | 9％ | 10％ | |
| Chemical compound of the present invention (a2) | 75°/35° | 144°/135° | 98°/133° | 51°/141° | Permeate/142 ° |
| Chemical compound of the present invention (b2) | 85°/46° | 148°/136° | 102°/138° | 62°/137° | Permeate/142 ° |
| Chemical compound of the present invention (c2) | 77°/37° | 145°/137° | 87°/137° | 54°/138° | Permeate/143 ° |
| The chemical compound of comparative example (d2) | 88°/40° | 140°/140° | 146°/145° | 145°/140° | 145°/142° |
| The chemical compound of comparative example (e2) | 97°/48° | 142°/142° | 144°/140° | 146°/142° | 143°/143° |
As show shown in the 2-30, utilize the water and oil repellant and the treating capacity of the processing powder body that the fluorinated copolymer of comparative example handles to improve pro rata, is that 6% water repellency when following and oil repellent are low by powder body that fluorinated copolymer of the present invention was covered in treating capacity, is to show the highest water and oil repellant at 7% o'clock in treating capacity.In treating capacity is to show hydrophilic oil repellent at 10% o'clock.Even if treating capacity is increased to more than 10%, oil repellent and hydrophilic also no longer change.Also see same result among the result shown in the following table 2-31.
Table 2-31: the result of embodiment 2-15 and comparative example 2-15
Each fluorinated copolymer is handled the water repellency and the hydrophilic result of the test of micropartical titanium oxide
| 6％ | 7％ | 8％ | 9％ | 10％ | |
| Chemical compound of the present invention (a2) | 3 | 5 | 3 | 2 | 1 |
| Chemical compound of the present invention (b2) | 3 | 5 | 3 | 2 | 1 |
| Chemical compound of the present invention (c2) | 3 | 5 | 3 | 2 | 1 |
| The chemical compound of comparative example (d2) | 4 | 5 | 5 | 5 | 5 |
| The chemical compound of comparative example (e2) | 4 | 5 | 5 | 5 | 5 |
The guide look of embodiment 2-1～2-15 and comparative example 2-1～2-15 is shown in table 2-32.
The guide look of table 2-32 embodiment and comparative example
Embodiment estimates the processing powder body of the minimum amount of coating that can obtain hydrophilic oil repellent.Comparative example is to use the powder body that is covered by the hydrophilic processing of refusing the treating capacity equivalent of oil processing powder body with embodiment.
Table 2-33: usability/fitness test result
(suppressing the checking of the moisture retention that effect produced by moisture loss)
After being coated on surface-treated powder of the present invention on the skin, utilizing following method to verify whether to have by having moistening effect and suppress the effect that moisture scatters and disappears from skin.Sample is to use the processing powder body through above-mentioned usability and fitness test.Test method: closed coating 10% sodium lauryl sulfate solution 2 hours at 30 preceding crook of the arm side seals, make the pachylosis model with sensory test person of healthy skin.The sample that is coated with is to make vaseline (Ri Xinglika (Nikko Rica) limited company): the mixture of lining powder body=1: 1 weight %.Sample is tested the powder body before the lining of each embodiment as non-lining powder body as a comparison.In addition, blank is only to be coated with vaseline.In pachylosis portion the coated face of 2cm * 4cm is set, at 2mg/cm
2Condition under be coated with said sample.Sooner or later respectively carry out 1 this operation every day, carried out continuously 5 days, re-uses the cutin moisture that Skicon-200 (IBS limited company) measures skin.Moistening effect is to obtain with the form of relative conductivity by calculating as described below to be coated with ratio preceding and the low frequency electric conductivity of coating after 5 days.In addition, pachylosis is to cause that because of the in disorder institute of skin ridge (cristae cutis) with sulci of skin (sulci cutis) smooth feeling of skin surface or rough sense are to ask sensory test person oneself to estimate.As followsly metewand is quantized and obtain aggregate value.Show the result in table 2-34.
Low frequency electric conductivity * 100 (%) before low frequency electric conductivity/coating after relative conductivity=coating
Table 2-34: moisture loss suppresses the effect test result: relative conductivity
As blank only use vaseline the time relative conductivity be 102%.As show shown in the 2-34, suppress effect by the visible moisture loss of the powder body that fluorinated copolymer of the present invention was covered.
[embodiment 2-16～2-38 and comparative example 2-16～2-38]
Then, the embodiment to the cosmetics that are mixed with surface-treated powder of the present invention describes.Based on each composition of following table, make various cosmetics by following method for making.
In addition, about the cosmetics that each embodiment and comparative example obtained, finish effect, cosmetic persistence at usability, cosmetic, for 20 professional sensory test persons are respectively prepared in each evaluation, please it make and apply some make up 1 day, and estimate according to the metewand shown in following table 2-35～table 2-37, whole sensory test persons' summation score is obtained divided by 20 to mark.In addition, the assessment item of usability is to estimate easily smearing property and smoothness.
Table 2-35: the evaluation of usability
| Benchmark | Scoring |
| Usability is very good | ◎ |
| Usability is good | ○ |
| Usability is common | ● |
| Usability is poor | △ |
| The non-constant of usability | × |
Table 2-36: make up and finish Evaluation on effect
| Benchmark | Scoring |
| Sensation produces effect very much | ◎ |
| Feel to produce effect | ○ |
| Sensation produces effect slightly | ● |
| Only feel small effect | △ |
| Sensation to no effect | × |
About finishing the project of effect, at making up and the skin care cosmetics are to estimate the uniformity of finishing effect, protection, the reflecting feel of nature, the uniformity of cosmetic film, at the hidroschesis cosmetics is to estimate to have or not the adhesion sense, have or not greasy feeling, is to estimate reflecting feel, dry feeling, smoothness, easy comb property at cosmetic hair.
Table 2-37: the evaluation of cosmetic persistence
| Benchmark | Scoring |
| Sensation produces effect very much | ◎ |
| Feel to produce effect | ○ |
| Sensation produces effect slightly | ● |
| Only feel small effect | △ |
| Sensation to no effect | × |
The project of cosmetic muffin is made as and prevents colour of skin dimness, prevents that secondary from adhering to (gamut), preventing glossy these 3 projects.In addition, be to estimate to be difficult for fissility at the manicure product.
The manufacturing of (embodiment 2-16 and comparative example 2-16) muffin
Make the muffin of forming shown in the table 2-38 by following method.Evaluation result is shown in table 2-39.
Table 2-38
| Composition | Weight portion |
| (1) sericite (5% item for disposal of embodiment 2-1 and comparative example 2-1) | 35.0 |
| (2) Talcum (5% item for disposal of embodiment 2-14 and comparative example 2-14) | To 100.0 |
| (3) silicone-treated titanium oxide | 8.5 |
| (4) silicone-treated yellow iron oxide | 3.5 |
| (5) silicone-treated red iron oxide | 1.8 |
| (6) silicone-treated black iron oxide | 0.2 |
| (7) hydroxyapatite | 5.0 |
| (8) myristic acid octyl group dodecyl ester | 4.0 |
| (9) squalane | 3.5 |
| (10) methyl phenyl silicone | 1.5 |
| (11) antiseptic | In right amount |
| (12) spice | In right amount |
(method for making)
Pulverize with mentioned component (1)～(7) mixing and by pulverizer.It is transferred in the high speed blender, adds the further mix homogeneously of material that composition (8)～(12) heating mix homogeneously is got.It is fed pulverizer, sieve and after making the granularity unanimity, the surface pressing with 10MPa in aluminium ware carries out compression molding, make dual-purpose muffin.
For above-mentioned foundation cream piece, open the contact angle that oil repellent test method(s) in the water of being put down in writing in the 2003-253077 communique is measured squalane by the Japan Patent spy through press molding.
Table 2-39
| Assessment item | Chemical compound (a2) | Chemical compound (b2) | Chemical compound (c2) | Chemical compound (d2) | Chemical compound (e2) |
| Usability | ○ | ○ | ◎ | △ | △ |
| Finish the uniformity of effect | ○ | ○ | ◎ | ● | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
| Oil repellent in the water | 66° | 72° | 67° | 36° | 20° |
The manufacturing of (embodiment 2-17 and comparative example 2-17) oil-in-water type foundation cream
Make the w/o type foundation emulsion of forming shown in the table 2-40 by following method.Evaluation result is shown in table 2-41.
Table 2-40
| Composition | Weight portion |
| (1) decamethylcyclopentaandoxane | 20.0 |
| (2) vaseline | 0.5 |
| (3) methyl phenyl silicone | 2.3 |
| (4) squalane | 4.2 |
| (5) different n-nonanoic acid isotridecyl ester | 4.5 |
| (6) polyether modified silicone * 11 | 3.0 |
| (7) silicone-treated red iron oxide | 1.3 |
| (8) silicone-treated yellow iron oxide | 2.4 |
| (9) silicone-treated black iron oxide | 0.1 |
| (10) silicone-treated titanium oxide | 8.0 |
| (11) silicone-treated Talcum | 2.5 |
| (12) ethanol | 5.0 |
| (13) 1,3 butylene glycol | 5.0 |
| (14) sodium chloride | 2.0 |
| (15) purified water | To 100.0 |
| (16) Amihope LL (5% item for disposal of embodiment 2-9 and comparative example 2-9) | 5.0 |
| (17) antiseptic | In right amount |
| (18) spice | In right amount |
* 11 KF-6038 (SHIN-ETSU HANTOTAI's chemical industry system)
(method for making)
Mentioned component (7)～(11) are pre-mixed pulverizing.To under 70 ℃, composition (1)～(6) being dissolved equably the mixture of composition (7)～(11) that adding crushes in advance in the oil phase that mixes, and utilize the homodisperse machine to disperse equably.Will be under 70 ℃ with composition (12)～(17) equably the water that forms of mixed dissolution slowly be added in the above-mentioned oil phase, utilize the homogenizer homodisperse after, cool off, add composition (18) and granulate and become emulsified particle, make foundation emulsion.
Table 2-41
* 12 quality stability are to place for 1 week afterwards to observe viscosity and separation, sedimentation in 50 ℃ temperature chamber.Being designated as of no cosmetic variation is good.
The manufacturing of (embodiment 2-18 and comparative example 2-18) eye shadow
Make the eye shadow of forming shown in the table 2-42 by following method.Evaluation result is shown in table 2-43.
Table 2-42
| Composition | Weight portion |
| 1. decamethylcyclopentaandoxane | 25.0 |
| 2. dimethyl polysiloxane (6cs) | 10.0 |
| 3. polyether modified silicone * 13 | 2.0 |
| 4.PEG (10) Laurel ether | 0.5 |
| 5. titanium oxide (5% item for disposal of embodiment 2-2 and comparative example 2-2) | 2.5 |
| 6. red iron oxide (6% item for disposal of embodiment 2-4 and comparative example 2-4) | 3.5 |
| 7. pearlescent pigment (5% item for disposal of embodiment 2-8 and comparative example 2-8) | 6.0 |
| 8. sodium chloride | 2.0 |
| 9. propylene glycol | 8.0 |
| 10. antiseptic | In right amount |
| 11. spice | In right amount |
| 12. purified water | To 100.0 |
* 13 KF6026 (SHIN-ETSU HANTOTAI's chemical industry system)
(method for making)
(1) with composition 1～4 mixed dissolution.
(2) composition 5～10 and composition 12 are mixed also dispersion equably.
(3) mixture that under agitation (2) is obtained slowly is added in the mixture that (1) obtained, and carries out emulsifying and adding ingredient 11 and obtains eye shadow.
Table 2-43
The manufacturing of the solid shape foundation cream of (embodiment 2-19 and comparative example 2-19) oiliness
Make the solid shape foundation cream of the oiliness of forming shown in the table 2-44 by following method.Evaluation result is shown in table 2-45.
Table 2-44
| Composition | Weight portion |
| (1) isopropyl palmitate | 20.0 |
| (2) spermol | 7.0 |
| (3) squalane | 15.5 |
| (4) polyglycereol three isostearates | 5.0 |
| (5) the different paraffin of volatile liquid | To 100.0 |
| (6) ceresine | 3.8 |
| (7) candelilla wax | 5.5 |
| (8) red iron oxide (6% item for disposal of embodiment 2-4 and comparative example 2-4) | 0.8 |
| (9) titanium oxide (5% item for disposal of embodiment 2-2 and comparative example 2-2) | 11.5 |
| (10) Talcum (5% item for disposal of embodiment 2-14 and comparative example 2-14) | 8.0 |
| (11) antiseptic | In right amount |
| (12) spice | In right amount |
(method for making)
Mentioned component (8)～(10) are pre-mixed pulverizing.To under 85 ℃, adding composition (8)～(11) crush in advance in the oil phase that composition (1)～(7) mixed dissolution forms, and utilize the homodisperse machine to disperse equably.To wherein adding spice, be filled in the metalware, make the solid shape foundation cream of oiliness and cool off.
Table 2-45
| Assessment item | Chemical compound (a2) | Chemical compound (b2) | Chemical compound (c2) | Chemical compound (d2) | Chemical compound (e2) |
| Usability | ◎ | ○ | ○ | △ | × |
| Finish the uniformity of effect | ○ | ◎ | ◎ | △ | × |
| The cosmetic persistence | ○ | ○ | ○ | △ | △ |
The manufacturing of (embodiment 2-20 and comparative example 2-20) oil-in-water type sunscreen cream
Make the oil-in-water type sunscreen cream of forming shown in the table 2-46 by following method.Evaluation result is shown in table 2-47.
Table 2-46
| Composition | Weight portion |
| 1. the different paraffin of volatile liquid (Fancol ID) | 15.0 |
| 2. polydimethylsiloxane (6cs) | 3.0 |
| 3. isononyl isononanoate | 4.5 |
| 4. spermol | 1.0 |
| 5. squalane | 5.0 |
| 6. polyethylene glycol mono stearate (4EO) | 1.0 |
| 7. poly-Semen Ricini linoleic acid six polyglycerin ester | 3.5 |
| 8. micropartical titanium oxide aqueous dispersion * 14 | 10.0 |
| 9. micropartical Zinc oxide water dispersion * 15 | 15.0 |
| 10. purified water | To 100.0 |
| 11. glycerol | 5.0 |
| 12.1, the 3-butanediol | 5.0 |
| 13. ketopyrrolidine sodium formate | 2.5 |
| 14. antiseptic | In right amount |
| 15. spice | In right amount |
* 14 10% of embodiment 2-6 and comparative example 2-6 handled micropartical titanium oxide and purified water disperse in sand mill with the composition of 30: 70 (weight portion) and make dispersion.Pigment-dispersing ability and storage stability height by the surface-treated powder that specific fluorinated copolymer of the present invention was covered.
* 15 9% of embodiment 2-7 and comparative example 2-7 handled micropartical zinc oxide and purified water disperse in sand mill with the composition of 35: 65 (weight portion) and make dispersion.Pigment-dispersing ability and storage stability height by the surface-treated powder that specific fluorinated copolymer of the present invention was covered.
(method for making)
The oil-phase component of composition (1)～(7) is dissolved down at 75 ℃.The water-phase component of composition (8)～(14) is dissolved dispersion down at 75 ℃, be added into after the homogenization in the oil-phase component, carry out emulsifying with homogenizer.Add composition (15) at last and cool off and make sunscreen cream.
Table 2-47
The manufacturing of (embodiment 2-21 and comparative example 2-21) eye-liner
Make the eye-liner of forming shown in the table 2-48 by following method.Evaluation result is shown in table 2-49.
Table 2-48
| Composition | Weight portion |
| (1) decamethylcyclopentaandoxane | 25.0 |
| (2) dimethyl polysiloxane (6cs) | 4.0 |
| (3) Simmondsia chinensis oil | 2.5 |
| (4) polyether modified silicone * 16 | 1.0 |
| (5) black iron oxide (5% item for disposal of embodiment 2-5 and comparative example 2-5) | 20.0 |
| (6) ethanol | 5.0 |
| (7) antiseptic | In right amount |
| (8) purified water | To 100.0 |
* 16 KF6026 (SHIN-ETSU HANTOTAI's chemical industry system)
(method for making)
(1) composition 1～4 is mixed under 70 ℃.
(2) composition 5～8 is heated to 70 ℃ and mixed dissolution, adds composition (5) and dispersion equably.
(3) mixture that under agitation (2) is obtained slowly is added in the mixture that (1) obtained, and carries out emulsifying and obtains eye-liner.
Table 2-49
The manufacturing of (embodiment 2-22 and comparative example 2-22) lipstick
Make the lipstick of forming shown in the table 2-50 by following method.Evaluation result is shown in table 2-51.
Table 2-50
| Composition | Weight portion |
| (1) malic acid two different stearyl esters | 15.0 |
| (2) three isooctyl acid glyceride | To 100.0 |
| (3) glutamic acid plant sterol octyldodecanol | 15.0 |
| (4) Brazil wax | 3.5 |
| (5) candelilla wax | 5.5 |
| (6) ceresine | 5.0 |
| (7) titanium oxide (5% item for disposal of embodiment 2-2 and comparative example 2-2) | 8.0 |
| (8) red No. 202 (9% item for disposal of embodiment 2-10 and comparative example 2-10) | 0.7 |
| (9) black iron oxide (5% item for disposal of embodiment 2-5 and comparative example 2-5) | 0.2 |
| (10) antiseptic | In right amount |
(method for making)
(1) composition 7～9 is added in the composition 1, mixes and it is disperseed equably with roller.
(2) with behind other composition heating mixed dissolution, add mentioned component (1) and utilize homogenizer to disperse equably.
(3) after the degassing, pour in the mould and obtain lip stick.
Table 2-51
| Assessment item | Chemical compound (a2) | Chemical compound (b2) | Chemical compound (c2) | Chemical compound (d2) | Chemical compound (e2) |
| Usability | ◎ | ○ | ○ | △ | △ |
| Finish the uniformity of effect | ○ | ○ | ◎ | △ | × |
| The cosmetic persistence | ◎ | ◎ | ◎ | △ | △ |
The manufacturing of (embodiment 2-23 and comparative example 2-23) lip coat
Make the lip coat of forming shown in the table 2-52 by following method.Evaluation result is shown in table 2-53.
Table 2-52
| Composition | Weight portion |
| (1) PFPE (Fomblin HC-04) | 91.0 |
| (2) silicon dioxide (Aerosil R-972) * 17 | 2.0 |
| (3) micropartical titanium oxide (10% item for disposal of embodiment 2-15 and comparative example 2-15) | 6.0 |
| (4) glycerol | 1.0 |
* 17 methods of mixing by embodiment 2-1 and comparative example 2-1 have been carried out the surface-treated material to be respectively each fluorochemical (a2)～(e2) of 5%.
(method for making)
In composition (1) adding ingredient (2) and composition (3) and disperse equably after, add composition (4) and make lip coat.
Table 2-53
| Assessment item | Chemical compound (a2) | Chemical compound (b2) | Chemical compound (c2) | Chemical compound (d2) | Chemical compound (e2) |
| Usability | ○ | ○ | ○ | ○ | ● |
| Finish the uniformity of effect | ○ | ◎ | ◎ | △ | × |
| The cosmetic persistence | ◎ | ◎ | ◎ | △ | ○ |
| Anti-transfer printing * 18 | ○ | ○ | ○ | × | △ |
* 18 treat that each sensory test person smears the lipstick of embodiment 2-22 and comparative example 2-22 after, observe when being coated with this lip coat lipstick to the bat printing state of cup.Be not designated as zero with what bat printing took place, will the △ that be designated as of bat printing be arranged slightly, with take place being designated as of bat printing *.
The manufacturing of (embodiment 2-24 and comparative example 2-24) oil-in-water type foundation emulsion
Make the O/W type foundation emulsion of forming shown in the table 2-54 by following method.Evaluation result is shown in table 2-55.
Table 2-54
| Composition | Weight portion |
| (1) stearic acid | 1.5 |
| (2) spermol | 1.0 |
| (3) Tween-81 (3EO) | 1.0 |
| (4) Span-83 | 1.0 |
| (5) liquid paraffin | 5.0 |
| (6) 2 ethyl hexanoic acid glyceride | 5.0 |
| (7) glycerol | 5.0 |
| (8) 1,3 butylene glycol | 5.0 |
| (9) acrylic acid-alkyl methacrylate (C 10～30) copolymer | 0.05 |
| (10) locust bean gum | 0.2 |
| (11) triethanolamine | 0.8 |
| (12) antiseptic | In right amount |
| (13) purified water | To 100.0 |
| (14) titanium oxide (5% item for disposal of embodiment 2-2 and comparative example 2-2) | 5.0 |
| (15) yellow iron oxide (6% item for disposal of embodiment 2-3 and comparative example 2-3) | 1.0 |
| (16) red iron oxide (6% item for disposal of embodiment 2-4 and comparative example 2-4) | 0.3 |
| (17) black iron oxide (5% item for disposal of embodiment 2-5 and comparative example 2-5) | 0.1 |
| (18) Amihope LL (5% item for disposal of embodiment 2-9 and comparative example 2-9) | 5.0 |
(method for making)
A: with composition (1)～(6) heating for dissolving.
B: with composition (7)～(13) equably after the heating for dissolving, add composition (14)～(18) and mix equably.
C: in the mixture that A obtained, add the mixture that B obtained, make foundation emulsion after the cooling.
Table 2-55
The manufacturing of (embodiment 2-25 and comparative example 2-25) colour of skin emulsion
Make the colour of skin emulsion of forming shown in the table 2-56 by following method.Evaluation result is shown in table 2-57.
Table 2-56
| Composition | Weight portion |
| (1) N-stearyl-L-glutamic acid | 0.5 |
| (2) spermol | 0.5 |
| (3) polyoxyethylene (10 moles) monostearate | 0.8 |
| (4) ten polyglycereol list isostearates | 1.0 |
| (5) Span-83 | 0.4 |
| (6) methyl phenyl silicone | 5.0 |
| (7) glycerol | 5.0 |
| (8) 1,3 butylene glycol | 5.0 |
| (9) Xanthan gum | 0.1 |
| (10) carrageenin | 0.05 |
| (11) triethanolamine | 1.0 |
| (12) antiseptic | In right amount |
| (13) purified water | To 100.0 |
| (14) titanium oxide (5% item for disposal of embodiment 2-2 and comparative example 2-2) | 2.0 |
| (15) yellow iron oxide (5% item for disposal of embodiment 2-3 and comparative example 2-3) | 1.0 |
| (16) red iron oxide (6% item for disposal of embodiment 2-4 and comparative example 2-4) | 0.5 |
| (17) black iron oxide (5% item for disposal of embodiment 2-5 and comparative example 2-5) | 0.1 |
| (18) Talcum (5% item for disposal of embodiment 2-14 and comparative example 2-14) | 3.0 |
(method for making)
A: with composition (1)～(6) heating for dissolving.
B: with composition (7)～(13) equably after the heating for dissolving, add composition (14)～(18) and mix equably.
C: add the mixture that B obtained in the mixture that A obtained, the cooling back obtains colour of skin emulsion.
Table 2-57
The manufacturing of (embodiment 2-26 and comparative example 2-26) manicure product
Make the manicure product of forming shown in the table 2-58 by following method.Evaluation result is shown in table 2-59.
Table 2-58
| Composition | Weight portion |
| (1) NC Nitroncellulose | 10.0 |
| (2) alkyd resins | 10.0 |
| (3) acetyl tributyl citrate | 4.0 |
| (4) dl-Camphora | 1.0 |
| (5) organically-modified Strese Hofmann's hectorite. | 1.0 |
| (6) ethyl acetate | 20.0 |
| (7) butyl acetate | To 100.0 |
| (8) isopropyl alcohol | 5.0 |
| (9) red No. 202 (9% item for disposal of embodiment 2-10 and comparative example 2-10) | 0.1 |
| (10) titanium oxide (5% item for disposal of embodiment 2-2 and comparative example 2-2) | 3.0 |
| (11) pearlescent pigment (5% item for disposal of embodiment 2-8 and comparative example 2-8) | 5.0 |
| (12) red iron oxide (6% item for disposal of embodiment 2-4 and comparative example 2-4) | 0.5 |
(method for making)
Utilizing dispersion machine that composition (1)～(9) are mixed stirs.To wherein adding composition (10)～(12) and utilizing dispersion machine to mix 10 minutes and make the manicure product, be filled in the vial.
Table 2-59
| Assessment item | Chemical compound (a2) | Chemical compound (b2) | Chemical compound (c2) | Chemical compound (d2) | Chemical compound (e2) |
| Usability | ○ | ○ | ○ | △ | △ |
| Finish the uniformity of effect | ○ | ○ | ○ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
In addition, the manicure product that are mixed with the surface-treated powder that is covered by specific fluorinated copolymer of the present invention can be in time through and form hard cake, dispersion stabilization is good.
The manufacturing of (embodiment 2-27 and comparative example 2-27) rouge
Make the rouge of forming shown in the table 2-60 by following method.Evaluation result is shown in table 2-61.
Table 2-60
| Composition | Weight portion |
| (1) sericite (3% item for disposal of embodiment 2-13 and comparative example 2-13) | 14.0 |
| (2) titanium oxide (5% item for disposal of embodiment 2-2 and comparative example 2-2) | 10.0 |
| (3) yellow iron oxide (5% item for disposal of embodiment 2-3 and comparative example 2-3) | 1.0 |
| (4) red iron oxide (6% item for disposal of embodiment 2-4 and comparative example 2-4) | 0.5 |
| (5) black iron oxide (5% item for disposal of embodiment 2-5 and comparative example 2-5) | 0.1 |
| (6) Talcum (5% item for disposal of embodiment 2-14 and comparative example 2-14) | To 100.0 |
| (7) Excel Mica JP-2 (three change into company well) | 7.0 |
| (8) PFPE (Fomblin HC-04) | 7.0 |
| (9) dimethyl polysiloxane (10CS) | 5.0 |
(method for making)
Composition (1)～(7) uniform mixing is pulverized.After wherein adding composition (8), (9) and uniform mixing, pulverize and make rouge.
Table 2-61
| Assessment item | Chemical compound (a2) | Chemical compound (b2) | Chemical compound (c2) | Chemical compound (d2) | Chemical compound (e2) |
| Usability | ○ | ○ | ○ | × | × |
| Finish the uniformity of effect | ◎ | ◎ | ○ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
The manufacturing of (embodiment 2-28 and comparative example 2-28) hidroschesis cosmetics
Make the bar-shaped hidroschesis cosmetics of forming shown in the table 2-62 by following method.Evaluation result is shown in table 2-63.
Table 2-62
| Composition | Weight portion |
| (1) Brazil wax | 1.0 |
| (2) ceresine | 6.0 |
| (3) paraffin | 3.0 |
| (4) sorbitan sesquialter isostearate | 2.5 |
| (5) 2 ethyl hexanoic acid cetyl | 27.0 |
| (6) squalane | 2.0 |
| (7) decamethylcyclopentaandoxane | To 100.0 |
| (8) polymeric aluminum chloride | 25.0 |
| (9) sericite (3% item for disposal of embodiment 2-13 and comparative example 2-13) | 5.0 |
| (10) silicone-treated Talcum | 8.0 |
| (11) Powder La Vie (three change into company well) | 5.0 |
| (12) micropartical zinc oxide (7% item for disposal of embodiment 2-12 and comparative example 2-12) | 2.0 |
| (13) antioxidant | In right amount |
| (14) spice | In right amount |
(method for making)
Composition (1)～(7) are heated and uniform dissolution.After wherein adding composition (8)～(13) and uniform mixing, add composition (14), cool off and make bar-shaped hidroschesis cosmetics.
Table 2-63
| Assessment item | Chemical compound (a2) | Chemical compound (b2) | Chemical compound (c2) | Chemical compound (d2) | Chemical compound (e2) |
| Usability | ○ | ◎ | ○ | × | × |
| Finish the uniformity of effect | ◎ | ◎ | ○ | △ | △ |
| The cosmetic persistence | ◎ | ◎ | ◎ | ○ | ○ |
The manufacturing of (embodiment 2-29 and comparative example 2-29) hair care breast
Make the hair care breast of forming shown in the table 2-64 by following method.Evaluation result is shown in table 2-65.
Table 2-64
| Composition | Weight portion |
| (1) glycol distearate | 1.0 |
| (2) liquid paraffin | 10.0 |
| (3) squalane | 5.0 |
| (4) stearyl alcohol | 1.5 |
| (5) dimethyl polysiloxane (10cs) | 3.0 |
| (6) stearic acid | 6.0 |
| (7) polyoxyethylene (3) stearyl alcohol | 4.5 |
| (8) polyoxyethylene (150) cetyl ether | 2.0 |
| (9) organic modified bentonite | 0.2 |
| (10) Amihope LL (5% item for disposal of embodiment 2-9 and comparative example 2-9) | 2.0 |
| (11) 1,3 butylene glycol | 6.0 |
| (12) antiseptic | In right amount |
| (13) purified water | To 100.0 |
| (14) spice | In right amount |
(method for making)
A: composition (1)～(9) are heated and uniform dissolution.
B: composition (10)～(13) heating is mixed dispersion.
C: add the mixture that B obtained and mix in the mixture that A obtained, the cooling back adds composition (14), cools off and makes the hair care breast.
Table 2-65
The manufacturing of (embodiment 2-30 and comparative example 2-30) colour of skin beautifying liquid
Make the colour of skin that table forms shown in the 2-66 beautifying liquid of preserving moisture by following method.Evaluation result is shown in table 2-67.
Table 2-66
| Composition | Weight portion |
| (1) purified water | To 100.0 |
| (2) acrylic acid-alkyl methacrylate (C 10～30) copolymer | 0.1 |
| (3) CVP Carbopol ETD2050 | 1.0 |
| (4) antiseptic | In right amount |
| (5) particulate titanium dioxide (10% item for disposal of embodiment 2-15 and comparative example 2-15) | 1.0 |
| (6) triethanolamine | 0.7 |
| (7) glycerol | 25.0 |
| (8) titanium oxide (5% item for disposal of embodiment 2-2 and comparative example 2-2) | 2.0 |
| (9) yellow iron oxide (5% item for disposal of embodiment 2-3 and comparative example 2-3) | 0.8 |
| (10) red iron oxide (6% item for disposal of embodiment 2-4 and comparative example 2-4) | 0.3 |
| (11) black iron oxide (5% item for disposal of embodiment 2-5 and comparative example 2-5) | 0.1 |
| (12) Talcum (5% item for disposal of embodiment 2-14 and comparative example 2-14) | 3.5 |
(method for making)
A: composition (1)～(4) heating after the uniform dissolution, is added composition (5) and homodisperse and mixes.Adding composition (6) neutralizes.
B: behind composition (8)～(12) uniform mixing, add composition (7) and uniform mixing.
C: in the mixture that A obtained, add the mixture that B obtained and mix, make the colour of skin beautifying liquid of preserving moisture.
Table 2-67
The manufacturing of (embodiment 2-31 and comparative example 2-31) aqueous eye shadow
Make the aqueous eye shadow of forming shown in the table 2-68 of aqueous by following method.Evaluation result is shown in table 2-69.
Table 2-68
| Composition | Weight portion |
| (1) purified water | To 100.0 |
| (2) acrylic acid-alkyl methacrylate (C 10～30) copolymer | 0.1 |
| (3) CVP Carbopol ETD2050 | 1.0 |
| (4) antiseptic | In right amount |
| (5) triethanolamine | 0.7 |
| (6) glycerol | 25.0 |
| (7) titanium oxide (5% item for disposal of embodiment 2-2 and comparative example 2-2) | 2.5 |
| (8) red iron oxide (6% item for disposal of embodiment 2-3 and comparative example 2-3) | 2.0 |
| (9) pearlescent pigment (5% item for disposal of embodiment 2-8 and comparative example 2-8) | 8.0 |
(method for making)
A: composition (1)～(4) heating after the uniform dissolution, is added composition (5) and uniform mixing.
B: behind composition (7)～(9) uniform mixing, add composition (6) and uniform mixing.
C: in the mixture that A obtained, add the mixture that B obtained and mix, make aqueous aqueous eye shadow.
Table 2-69
The manufacturing of (embodiment 2-32 and the comparative example 2-32) powder of whitening
Make the powder of forming shown in the table 2-70 of whitening by following method.Evaluation result is shown in table 2-71.
Table 2-70
| Composition | Weight portion |
| (1) L-magnesium L-ascorbyl-2-phosphate | 1.0 |
| (2) sodium citrate | 1.0 |
| (3) 1,3 butylene glycol | 5.0 |
| (4) glycerol | 5.0 |
| (5) purified water | To 100.0 |
| (6) methyl parahydroxybenzoate | 0.2 |
| (7) sericite (5% item for disposal of embodiment 2-1 and comparative example 2-1) | 5.0 |
| (8) Talcum (5% item for disposal of embodiment 2-14 and comparative example 2-14) | 0.1 |
| (9) organopolysiloxane elastomer powder | 3.0 |
| (10) partially crosslinked organopolysiloxane polymer * 19 | 5.0 |
| (11) silicone-treated red iron oxide | 0.5 |
| (12) three fluoro-alkyl dimethyl trimethyl silicane alcoxyl base esters of silicon acis | 3.0 |
* 19 KSG-16 (chemical industrial company of SHIN-ETSU HANTOTAI system)
(method for making)
A: composition (1)～(8) are mixed, disperseed.
B: with composition (9)～(12) uniform mixing.
C: the mixture that above-mentioned A obtained is mixed with the mixture that B is obtained, be filled in the container and obtain to whiten powder.
Table 2-71
The manufacturing of (embodiment 2-33 and comparative example 2-33) anti-Exposure to Sunlight frost
Make the anti-Exposure to Sunlight frost of forming shown in the table 2-72 by following method.Evaluation result is shown in table 2-73.
Table 2-72
* the compositions of 10 micropartical titanium oxide/purified water/glycerol=45/50/5 that 10% of embodiment 2-6 and comparative example 2-6 handled utilizes sand mill to disperse, and makes aqueous dispersion.The aqueous dispersion of embodiment can be not in time through and settlement separate, comparatively stable.The dispersion of the dispersion of comparative example does not go on, and fails to form even and stable dispersion.
(method for making)
A: with composition (3)～(6) heating, mixing.
B:, be added in the mixture that above-mentioned A obtains with behind composition (1) and (2) uniform mixing.
C: composition (7)～(12) are mixed, dissolved.
D: in the mixture that above-mentioned B obtained, add the mixture that C obtained, carry out emulsifying and obtain anti-Exposure to Sunlight frost.
Table 2-73
* 21 quality stability be in 50 ℃ temperature chamber, place 1 week the back observe the having that it's too late and separate of crystallization, the sedimentation of UV absorbent.The cosmetics of cosmetic variation such as no crystallization are designated as well.Crystallization took place and produces separation next day in the cosmetics that are mixed with the chemical compound (d2) of comparative example and processing powder body (e2), and quality stability is poor.
The manufacturing of (embodiment 2-34 and comparative example 2-34) anti-Exposure to Sunlight condensation
Make the anti-Exposure to Sunlight condensation of forming shown in the table 2-74 by following method.Evaluation result is shown in table 2-75.
Table 2-74
(method for making)
After composition (1)～(4) were heated to 80 ℃, adding ingredient (7) also utilized dispersion machine to disperse.Composition (5) and (6) are heated to 80 ℃ and dissolving.The composition (5) that adds in mentioned component through heating for dissolving neutralizes with (6).Composition (8) is mixed with (9) and be heated to 80 ℃.To above-mentioned these compositions that in neutral composition, slowly add, utilize homogenizer to carry out emulsifying and obtain anti-Exposure to Sunlight condensation.
Table 2-75
* 22 this preparation preserved 1 month down at 50 ℃.With the unconverted ◎ that is designated as of the character of outward appearance.
The cosmetics that are mixed with surface-treated powder of the present invention do not have the reactivity with water soluble polymer, have obtained stable formulation.
The manufacturing of (embodiment 2-35 and comparative example 2-35) wet forming muffin
Make the foundation cream of forming shown in the table 2-76 by following method.Evaluation result is shown in table 2-77.
Table 2-76
| Composition | Weight portion |
| (1) sericite (3% item for disposal of embodiment 2-13 and comparative example 2-13) | To 100.0 |
| (2) MW handles (hydrophilicity-imparting treatment) PMMA (three change into company well) | 10.0 |
| (3) titanium oxide (5% item for disposal of embodiment 2-2 and comparative example 2-2) | 12.0 |
| (4) yellow iron oxide (5% item for disposal of embodiment 2-3 and comparative example 2-3) | 2.5 |
| (5) red iron oxide (6% item for disposal of embodiment 2-4 and comparative example 2-4) | 0.8 |
| (6) black iron oxide (5% item for disposal of embodiment 2-5 and comparative example 2-5) | 0.3 |
| (7) p-methoxycinnamic acid-2-Octyl Nitrite | 3.0 |
| (8) polyoxyethylene (20 moles) hardened castor oil | 1.5 |
(method for making)
A: composition (7) and (8) are heated to 75 ℃ and dissolving equably.
B: utilize mixer that micronizing is carried out in composition (1)～(6) mixing.
C: one side utilizes mixer that above-mentioned B is stirred, and one side is added A and homodisperse.
D: with respect to the composition of the C of 100 weight portions, the purified water of adding 100 weight portions, uniform mixing and make pulp-like.
E: above-mentioned D is filled in the metalware, places absorbent paper and pressurization on the surface, remove a part of purified water.
F: above-mentioned F was placed 24 hours in 50 ℃ temperature chamber, remove purified water fully, obtain the wet forming muffin.
Table 2-77
The manufacturing of (embodiment 2-36 and comparative example 2-36) F/W emulsifying emulsion
Make the emulsion of forming shown in the table 2-78 by following method.Evaluation result is shown in table 2-79.
Table 2-78
| Composition | Weight portion |
| (1) PFPE (Fomblin HC/04:Solvay company) | 25.0 |
| (2) hydrogen fluorine ether (CF-76:3M company) | 10.0 |
| (3) silicone-treated Talcum | 1.5 |
| (4) ethanol | 8.0 |
| (5) glycerol | 3.5 |
| (6) micropartical zinc oxide (7% item for disposal of embodiment 2-12 and comparative example 2-12) | 5.0 |
| (7) purified water | To 100.0 |
| (8) antiseptic | In right amount |
(method for making)
A: with composition (1)～(3) uniform mixing and be heated to 50 ℃.
B: utilize homogenizer that composition (4)～(8) dispersing and dissolving is mixed, be heated to 50 ℃.
C: one side utilizes homogenizer that above-mentioned B is stirred, and one side is slowly added above-mentioned A and obtained F/W emulsifying emulsion.
Table 2-79
The manufacturing of (embodiment 2-37 and comparative example 2-37) W/F emulsifying emulsion
Make the emulsion of forming shown in the table 2-80 by following method.Evaluation result is shown in table 2-81.
Table 2-80
| Composition | Weight portion |
| (1) PFPE (Fomblin HC/04:Solvay company) | 45.0 |
| (2) hydrogen fluorine ether (CF-76:3M company) | 15.0 |
| (3) silicone-treated Talcum | 1.5 |
| (4) ethanol | 8.0 |
| (5) glycerol | 3.5 |
| (6) micropartical zinc oxide (7% item for disposal of embodiment 2-12 and comparative example 2-12) | 5.0 |
| (7) purified water | To 100.0 |
| (8) antiseptic | In right amount |
(method for making)
A: with composition (1)～(3) uniform mixing and be heated to 50 ℃.
B: utilize homogenizer that composition (4)～(8) dispersing and dissolving is mixed, be heated to 50 ℃.
C: one side utilizes homogenizer that above-mentioned A is stirred, and one side is slowly added above-mentioned B and obtained W/F emulsifying emulsion.
Table 2-81
The manufacturing of (embodiment 2-38 and comparative example 2-38) powder body emulsifying sunscreen cream
Make the emulsion of forming shown in the table 2-82 by following method.Evaluation result is shown in table 2-83.
Table 2-82
| Composition | Weight portion |
| (1) 2-Methylpentadecane | 20.0 |
| (2) different n-nonanoic acid isotridecyl ester | 7.0 |
| (3) dimethylsilyl silicon dioxide (Aerosil R972: Japanese A Erluoxier company) | 3.5 |
| (4) micropartical titanium oxide (10% item for disposal of embodiment 2-15 and comparative example 2-15) | 5.0 |
| (5) micropartical zinc oxide (7% item for disposal of embodiment 2-12 and comparative example 2-12) | 10.0 |
| (6) ethanol | 5.0 |
| (7) glycerol | 7.0 |
| (8) purified water | To 100.0 |
| (9) antiseptic | In right amount |
(method for making)
A: utilize dispersion machine with composition (1)～(3) uniform mixing, and be heated to 50 ℃.
B: composition (4)～(9) are heated to 50 ℃ and uniform mixing dispersion.
C: one side utilizes homogenizer that above-mentioned A is stirred, and one side is slowly added above-mentioned B and obtained powder body emulsifying sunscreen cream.
Table 2-83
[possibility of utilizing on the industry]
Surface-treated powder of the present invention is preferably and can be used as the used for cosmetic surface-treated powder, but it not only can be applicable to cosmetics, and the various fields such as the powder stuffing that also can be applicable to mix in ink, coating, resin masterbatch, the paper etc., ceramic material, magnetic material, rare earth, optical material, conductive material, voltage material.
Claims (19)
1. surface-treated powder, it is to desire to carry out the surface-treated powder that the surface of surface-treated powder particle forms with surface conditioning agent lining, it is characterized in that, described surface conditioning agent be must comprise the fluorochemical monomer shown in (a) following general formula (I) and (b) the monomeric monomer copolymerization that contains alkoxyl shown in the following general formula (II) and fluorinated copolymer;
CH
2＝C(-X)-C(＝O)-Y-[-(CH
2)
m-Z-]
p-(CH
2)
n-Rf (I)
In the formula, X is hydrogen atom, methyl, fluorine atom, chlorine atom, bromine atoms, iodine atom, CFX
1X
2Base, cyano group, carbon number be 1～20 straight chain shape or branch-like fluoro-alkyl, be substituted or the benzyl of non-replacement, be substituted or the phenyl of non-replacement; Y is-O-or-NH-; Z be Direct Bonding ,-S-or-SO
2-; Rf is that carbon number is 1～6 fluoro-alkyl; M is 1～10, and n is 0～10, and p is 0 or 1; Described CFX
1X
2In, X
1And X
2Be hydrogen atom, fluorine atom or chlorine atom;
CH
2＝C(X
1)-C(＝O)-O-(RO)
q-X
2 (II)
In the formula, X
1Be hydrogen atom or methyl; X
2It for hydrogen atom or carbon number 1～22 unsaturated or saturated hydrocarbyl; R is that carbon number that part or all of hydrogen atom can be replaced by hydroxyl is 2～4 alkylidene; Q is 1～50 integer.
2. surface-treated powder as claimed in claim 1 is characterized in that, in the described general formula (II), and X
2Be hydrogen atom.
3. surface-treated powder as claimed in claim 1 or 2 is characterized in that described surface-treated powder has water and oil repellant.
4. surface-treated powder as claimed in claim 1 or 2 is characterized in that described surface-treated powder has hydrophilic oil repellent.
5. as each described surface-treated powder in the claim 1～4, it is characterized in that the fluorinated copolymer that comprises the cross-linkable monomer shown in the following logical formula III in the constituent by described fluorinated copolymer is covered;
CH
2＝C(X
3)-C(＝O)-O-(R
1O)
q-C(＝O)-C(X
3)＝CH
2 (III)
In the formula, each X
3Be hydrogen atom or methyl; R
1The carbon number that can be replaced by hydroxyl for part or all of hydrogen atom is 2～10 alkylidene; Q is 1～50 integer.
6. as each described surface-treated powder in the claim 1～5, it is characterized in that the weight average molecular weight of described fluorinated copolymer is about 1000～about 1000000.
7. as each described surface-treated powder in the claim 1～6, it is characterized in that in the described fluorinated copolymer, fluorochemical monomer (a) is 100 weight portions, the monomer (b) that contains alkoxyl is 10～400 weight portions.
8. as each described surface-treated powder in the claim 1～7, it is characterized in that desire to carry out surface-treated powder body 100 weight portions with respect to described, the amount of coating of described fluorinated copolymer is 0.01～40 weight portion.
9. as each described surface-treated powder in the claim 1～8, it is characterized in that described surface conditioning agent also comprises more than one the chemical compound that is selected from the following chemical compound group;
Described chemical compound group: other fluorochemical, organopolysiloxane, alkyl silane, polyether modified silicane, organic titanate, polyolefin, hydrolecithin, acylated amino acid, acid ester oil, fatty acid and dextrin fatty acid ester beyond the described fluorinated copolymer; Described hydrolecithin comprises the hydrolecithin of salt form; Described acylated amino acid comprises the acylated amino acid of salt form or compositions form; Described fatty acid comprises the fatty acid of salt form.
10. surface-treated powder as claimed in claim 9 is characterized in that, described fluorochemical is that carbon number is at least a in perfluoralkyl phosphate below 6 and perfluoroalkyl silane, perfluoro polyether phosphate, the Perfluoropolyether silanes.
11. as each described surface-treated powder in the claim 1～10, it is characterized in that, by desiring to carry out surface-treated powder body 100 weight portions and be covered by more than one the chemical compound that is selected from the described chemical compound group of the described fluorinated copolymer of 0.01 weight portion～39.99 weight portions and 39.99 weight portions～0.01 weight portion with respect to described.
12., it is characterized in that described to desire to carry out the surface-treated powder body be the powder body that can be used for cosmetics as each described surface-treated powder in the claim 1～11.
13. surface-treated powder as claimed in claim 12 is characterized in that, the powder body that can be used for described cosmetics is the inorganic particle that can be used for cosmetics.
14. surface-treated powder as claimed in claim 13, it is characterized in that, described inorganic particle be in sericite, Muscovitum, Kaolin, Talcum, silicon dioxide, barium sulfate, boron nitride, titanium oxide, zinc oxide, ferrum oxide and the pearlescent pigment any or two or more.
15. surface-treated powder as claimed in claim 12 is characterized in that, the powder body that can be used for described cosmetics is the organic powder that can be used for cosmetics.
16. cosmetics is characterized in that, are mixed with each described surface-treated powder in the claim 1～15.
17. cosmetics as claimed in claim 16 is characterized in that, also comprise at least a as constituent in oiliness composition, water composition and the surfactant.
18., it is characterized in that, be any cosmetic in skin care cosmetics, cosmetic hair, cosmetic cosmetics and the uvioresistant cosmetics as claim 16 or 17 described cosmetics.
19., it is characterized in that the goods form is any form in aqueous, emulsion form, white shape, solid shape, pasty state, gel, Powdered, multilamellar shape, Mu Sizhuan and the spray form as each described cosmetics in the claim 16～18.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008133521 | 2008-05-21 | ||
| JP2008-133521 | 2008-05-21 | ||
| PCT/JP2009/054377 WO2009142047A1 (en) | 2008-05-21 | 2009-03-03 | Surface-treated powder and cosmetic comprising the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102036650A true CN102036650A (en) | 2011-04-27 |
Family
ID=41339986
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2009801184599A Pending CN102036650A (en) | 2008-05-21 | 2009-03-03 | Surface-treated powder and cosmetic comprising the same |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20110110995A1 (en) |
| EP (1) | EP2289484A4 (en) |
| JP (1) | JPWO2009142047A1 (en) |
| CN (1) | CN102036650A (en) |
| WO (1) | WO2009142047A1 (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104167235A (en) * | 2014-07-25 | 2014-11-26 | 江苏通光光缆有限公司 | Conductive fiber cable |
| CN104169377A (en) * | 2012-03-23 | 2014-11-26 | 罗门哈斯公司 | Binder thickened with xanthan gum |
| CN107613950A (en) * | 2015-05-28 | 2018-01-19 | 堺化学工业株式会社 | Sebum adsorbent and the cosmetic preparation containing the sebum adsorbent |
| CN110879047A (en) * | 2019-12-05 | 2020-03-13 | 国网山东省电力公司电力科学研究院 | Method for testing contact angle of powder material |
| CN111163748A (en) * | 2017-07-31 | 2020-05-15 | 株式会社爱茉莉太平洋 | Cosmetic composition comprising pigment and method for preparing same |
| CN113736287A (en) * | 2021-08-23 | 2021-12-03 | 中国科学院上海硅酸盐研究所 | Super-hydrophilic self-cleaning graphene-based pearlescent pigment composite material and preparation method thereof |
| CN114561109A (en) * | 2022-01-29 | 2022-05-31 | 新疆德欣精细化工有限公司 | High-purity carbon black nano material based on powder pretreatment and preparation method thereof |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011088850A (en) * | 2009-10-22 | 2011-05-06 | Miyoshi Kasei Inc | Surface-treated powder and cosmetic comprising the same |
| FR2954150B1 (en) * | 2009-12-17 | 2012-03-16 | Oreal | USE OF ONE OR MORE PRESSURE-SENSITIVE ADHESIVE COMPOUNDS AS AN AGENT FOR THE TREATMENT OF HUMAN PERSPIRATION |
| CN102665668B (en) | 2009-12-24 | 2014-10-22 | 道康宁东丽株式会社 | Copolymer having carbosiloxane dendrimer structure, and composition and cosmetic containing the same |
| EP2516510B1 (en) | 2009-12-24 | 2017-01-25 | Dow Corning Toray Co., Ltd. | Surface-treatment agent for powder for use in cosmetic and cosmetic containing powder treated with the same |
| JP5490523B2 (en) * | 2009-12-26 | 2014-05-14 | 日本メナード化粧品株式会社 | Solid powder cosmetic |
| JP5582525B2 (en) * | 2010-03-18 | 2014-09-03 | 日本メナード化粧品株式会社 | Solid powder cosmetic |
| WO2012042570A1 (en) * | 2010-09-29 | 2012-04-05 | L'oreal | A cosmetic method for hiding skin imperfections |
| WO2012136607A1 (en) * | 2011-04-05 | 2012-10-11 | Akzo Nobel Chemicals International B.V. | Grafted particles for use in skin care applications |
| ITMI20110644A1 (en) * | 2011-04-14 | 2012-10-15 | Giuliani Spa | PROLONGED RELEASE SYSTEM FOR COSMETIC AGENTS |
| JP5889309B2 (en) * | 2011-08-29 | 2016-03-22 | Ａｇｃセイミケミカル株式会社 | Copolymers for cosmetics, surface treatment agents for cosmetic powders, cosmetic powders and cosmetics |
| JP5976523B2 (en) * | 2011-12-28 | 2016-08-23 | 富士フイルム株式会社 | Optical member set and solid-state imaging device using the same |
| US8697100B2 (en) * | 2012-01-23 | 2014-04-15 | Nikko Chemicals Co., Ltd. | Surface-treated powder and a method of producing it, and cosmetics comprising the surface-treated powder |
| JP5679502B2 (en) | 2012-02-28 | 2015-03-04 | 花王株式会社 | Cosmetics |
| JP5797618B2 (en) | 2012-08-22 | 2015-10-21 | 東レ・ダウコーニング株式会社 | Copolymer having carbosiloxane dendrimer structure, and composition and cosmetic containing the same |
| JP6092545B2 (en) | 2012-08-22 | 2017-03-08 | 東レ・ダウコーニング株式会社 | Copolymer having carbosiloxane dendrimer structure and hydrophilic group and use thereof |
| FR2996132B1 (en) * | 2012-10-02 | 2015-06-26 | Oreal | NOVEL COSMETIC USES OF DISPERSING POLYMERS IN ASSOCIATION WITH AT LEAST ONE NON-COLORING LOAD |
| FR2996133B1 (en) * | 2012-10-02 | 2015-06-26 | Oreal | NOVEL COSMETIC USES OF DISPERSING POLYMERS IN ASSOCIATION WITH AT LEAST ONE ACTIVE |
| FR2996131B1 (en) * | 2012-10-02 | 2015-06-26 | Oreal | NOVEL COSMETIC USES OF DISPERSING POLYMERS IN ASSOCIATION WITH AT LEAST ONE COLORING MATERIAL |
| FR2996134B1 (en) * | 2012-10-02 | 2015-06-26 | Oreal | COSMETIC COMPOSITIONS COMPRISING A DISPERSING POLYMER, AT LEAST ONE COLORING MATERIAL AND A HIGH WATER CONTENT |
| WO2015002620A1 (en) * | 2013-07-01 | 2015-01-08 | Eysi̇m İthalat İhracat Gida Tarim Ki̇myevi̇ Maddeler Otomoti̇v Taşimacilik Petrol Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇ | Nail polish (enamel) that has decreased toxicity, increased uv resistance and is self-shining in unlighted environments |
| JP2015051957A (en) * | 2013-09-09 | 2015-03-19 | ロレアル | Powdery cosmetic composition |
| JP6321957B2 (en) * | 2013-12-13 | 2018-05-09 | 花王株式会社 | Solid powder cosmetic |
| CN103819941A (en) * | 2014-02-12 | 2014-05-28 | 铜陵瑞莱科技有限公司 | Iron oxide red pigment containing balsamine pollen |
| JP7075241B2 (en) * | 2018-02-28 | 2022-05-25 | 東洋アルミエコープロダクツ株式会社 | Beautiful nail set and beautiful nail method |
| JP7101520B2 (en) * | 2018-04-12 | 2022-07-15 | 第一工業製薬株式会社 | Hydrophilic oil repellent |
| JP7073950B2 (en) | 2018-07-09 | 2022-05-24 | 日立金属株式会社 | Fluororesin powder manufacturing method |
| JP2021014412A (en) * | 2019-07-10 | 2021-02-12 | 三菱鉛筆株式会社 | Liquid cosmetic composition |
| EP4062896A4 (en) * | 2019-11-21 | 2023-12-27 | Miyoshi Kasei, Inc. | Glycerin dispersion and cosmetic |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60190705A (en) | 1984-03-12 | 1985-09-28 | Miyoshi Kasei:Kk | Cosmetic compounded with pigment surface-treated with hydrogenated lecithin |
| JPS60184571A (en) | 1984-03-01 | 1985-09-20 | Miyoshi Kasei:Kk | Pigment having surface treated with hydrogenated lecithin |
| JPS62250074A (en) | 1986-04-21 | 1987-10-30 | Daito Kasei Kogyo Kk | Water-repellent, oil-repellent pigment and production thereof |
| JPS63179972A (en) | 1987-01-21 | 1988-07-23 | Miyoshi Kasei:Kk | Polyolefin resin treated pigment and cosmetic |
| JPH02218603A (en) | 1989-02-21 | 1990-08-31 | Shiseido Co Ltd | Cosmetic |
| JPH0818950B2 (en) * | 1992-05-01 | 1996-02-28 | 花王株式会社 | Cosmetics |
| DE69432228T2 (en) | 1993-12-29 | 2004-01-22 | Daikin Industries, Ltd. | FLUORED OIL-IN-WATER EMULSION FOR SURFACE TREATMENT |
| DE69624923T2 (en) | 1995-08-11 | 2003-08-21 | Daikin Ind Ltd | ORGANIC FLUORINE POLYMERS CONTAINING SILICON AND THEIR USE |
| JP2000290640A (en) | 1999-02-04 | 2000-10-17 | Daikin Ind Ltd | Agent for repelling water and oil |
| JP4602506B2 (en) * | 1999-07-08 | 2010-12-22 | 三好化成株式会社 | Novel coated powder having super-dispersibility and cosmetics containing the same |
| JP4149378B2 (en) * | 2001-06-29 | 2008-09-10 | 株式会社資生堂 | Composite powder and external preparation for skin containing the same |
| WO2003047535A1 (en) * | 2001-12-05 | 2003-06-12 | Pola Chemical Industries Inc. | External preparation for the skin and copolymer to be used therein |
| JP2003253077A (en) | 2002-02-27 | 2003-09-10 | Daikin Ind Ltd | Polymer blend and surface treatment agent |
| JP4145681B2 (en) | 2002-05-27 | 2008-09-03 | 三好化成株式会社 | Powder surface-treated with specific acid ester oil and cosmetic composition containing the same |
| JP4212924B2 (en) * | 2002-08-08 | 2009-01-21 | 花王株式会社 | Composite polymer particles and process for producing the same |
| JP4426859B2 (en) | 2004-02-02 | 2010-03-03 | ポーラ化成工業株式会社 | Polymer composition for film formation |
| JP2006008757A (en) * | 2004-06-23 | 2006-01-12 | Kao Corp | Oil-absorbing swellable polymer particle |
| JP2007210939A (en) * | 2006-02-09 | 2007-08-23 | Asahi Glass Co Ltd | Powder for cosmetic and cosmetic |
| JP2007238690A (en) | 2006-03-07 | 2007-09-20 | Daito Kasei Kogyo Kk | Water- and oil-repellent pigment and cosmetic containing the same |
| JP2007269642A (en) * | 2006-03-30 | 2007-10-18 | Daikin Ind Ltd | Cosmetic containing fluoroacrylate polymer |
| JP2008214229A (en) | 2007-03-01 | 2008-09-18 | Miyoshi Kasei Inc | Surface-treated powder coated with specific perfluoropolyether-modified aminosilane and cosmetic comprising the same formulated therein |
| JP2008050620A (en) | 2007-10-25 | 2008-03-06 | Daikin Ind Ltd | Copolymer for cosmetic |
-
2009
- 2009-03-03 CN CN2009801184599A patent/CN102036650A/en active Pending
- 2009-03-03 JP JP2010512956A patent/JPWO2009142047A1/en active Pending
- 2009-03-03 US US12/993,346 patent/US20110110995A1/en not_active Abandoned
- 2009-03-03 EP EP09750409.6A patent/EP2289484A4/en not_active Withdrawn
- 2009-03-03 WO PCT/JP2009/054377 patent/WO2009142047A1/en active Application Filing
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104169377A (en) * | 2012-03-23 | 2014-11-26 | 罗门哈斯公司 | Binder thickened with xanthan gum |
| CN104167235A (en) * | 2014-07-25 | 2014-11-26 | 江苏通光光缆有限公司 | Conductive fiber cable |
| CN107613950A (en) * | 2015-05-28 | 2018-01-19 | 堺化学工业株式会社 | Sebum adsorbent and the cosmetic preparation containing the sebum adsorbent |
| CN111163748A (en) * | 2017-07-31 | 2020-05-15 | 株式会社爱茉莉太平洋 | Cosmetic composition comprising pigment and method for preparing same |
| CN111163748B (en) * | 2017-07-31 | 2023-04-21 | 株式会社爱茉莉太平洋 | Cosmetic composition comprising pigment and method for preparing the same |
| CN110879047A (en) * | 2019-12-05 | 2020-03-13 | 国网山东省电力公司电力科学研究院 | Method for testing contact angle of powder material |
| CN113736287A (en) * | 2021-08-23 | 2021-12-03 | 中国科学院上海硅酸盐研究所 | Super-hydrophilic self-cleaning graphene-based pearlescent pigment composite material and preparation method thereof |
| CN114561109A (en) * | 2022-01-29 | 2022-05-31 | 新疆德欣精细化工有限公司 | High-purity carbon black nano material based on powder pretreatment and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| US20110110995A1 (en) | 2011-05-12 |
| WO2009142047A1 (en) | 2009-11-26 |
| EP2289484A4 (en) | 2014-08-13 |
| EP2289484A1 (en) | 2011-03-02 |
| JPWO2009142047A1 (en) | 2011-09-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102036650A (en) | Surface-treated powder and cosmetic comprising the same | |
| JP5001486B2 (en) | Oil dispersion of powder having super-dispersion stability and cosmetics containing the same | |
| JP6885788B2 (en) | Elastomer | |
| JP2008214229A (en) | Surface-treated powder coated with specific perfluoropolyether-modified aminosilane and cosmetic comprising the same formulated therein | |
| JP2011088850A (en) | Surface-treated powder and cosmetic comprising the same | |
| WO2008012922A1 (en) | Powdery cosmetic | |
| WO2014010671A1 (en) | Method for producing coated inorganic particles | |
| JP5497314B2 (en) | Oily cosmetics | |
| JP2006213651A (en) | Solid powder cosmetic | |
| JP2005306847A (en) | Cake powder cosmetic | |
| JP3492788B2 (en) | Makeup cosmetics | |
| JP2021155383A (en) | Cosmetic powder, colorfastness improver, and colorfastness improvement method | |
| JP6012983B2 (en) | Coated powder and method for producing the same | |
| JP6114066B2 (en) | Solid powder cosmetic | |
| JP2008050388A (en) | Water-repellent and oil-repellent pigment and cosmetic containing the same | |
| JP2008214267A (en) | Manufacturing method of powdery cosmetic | |
| JP7306952B2 (en) | Powdered cosmetic and method for producing the same | |
| CN108078800B (en) | Oily cosmetic | |
| JP3492790B2 (en) | Makeup cosmetics | |
| JP4328103B2 (en) | Cosmetics | |
| JP5584005B2 (en) | Iron oxide / organopolysiloxane hybrid powder, method for producing the same, and cosmetics containing the same | |
| JP2010030952A (en) | Treated powder and cosmetic | |
| JP2020164458A (en) | Oil-in-water emulsion cosmetic | |
| JP2005171145A (en) | Disperse composition and cosmetic in which the same composition is formulated | |
| JP3461972B2 (en) | Makeup cosmetics |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20110427 |